Canonical Allele Identifier: CA373177082

Gene: APTX

Linked Data

• ClinVar Variation Id: 1459533
• ClinVar RCV Id: RCV001959044
• dbSNP Id: rs2118681567
• MyVariant Identifiers: chr9:g.32984705C>A (hg19) ; chr9:g.32984707C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.32984707C>A , CM000671.2:g.32984707C>A	GRCh38
NC_000009.11:g.32984705C>A , CM000671.1:g.32984705C>A	GRCh37
NC_000009.10:g.32974705C>A	NCBI36
NG_012821.1:g.21922G>T
NG_012821.2:g.45425G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000309615.8:c.532G>T	ENSP00000311547.4:p.Glu178Ter
ENST00000379817.7:c.694G>T MANE Select	ENSP00000369145.2:p.Glu232Ter
ENST00000379819.6:c.694G>T	ENSP00000369147.2:p.Glu232Ter
ENST00000379825.7:c.694G>T	ENSP00000369153.3:p.Glu232Ter
ENST00000397172.8:c.478G>T	ENSP00000380357.4:p.Glu160Ter
ENST00000436040.7:c.532G>T	ENSP00000400806.4:p.Glu178Ter
ENST00000460940.6:c.*388+1264G>T	ENSP00000418311.1:n.*388+1264G>T
ENST00000463596.6:c.694G>T	ENSP00000419846.1:p.Glu232Ter
ENST00000464632.6:c.*424G>T	ENSP00000418069.2:n.*424G>T
ENST00000465003.6:c.*424G>T	ENSP00000419430.2:n.*424G>T
ENST00000467331.6:c.*539G>T	ENSP00000418733.1:n.*539G>T
ENST00000468275.6:c.694G>T	ENSP00000420263.2:p.Glu232Ter
ENST00000472896.6:c.*488G>T	ENSP00000417804.2:n.*488G>T
ENST00000474658.7:c.*137G>T	ENSP00000417750.3:n.*137G>T
ENST00000476858.6:c.532G>T	ENSP00000419042.2:p.Glu178Ter
ENST00000477119.2:c.577G>T	ENSP00000417649.2:p.Glu193Ter
ENST00000478279.6:c.*321G>T	ENSP00000419597.2:n.*321G>T
ENST00000479656.6:c.*539G>T	ENSP00000420071.1:n.*539G>T
ENST00000482687.6:c.*388+1264G>T	ENSP00000419289.2:n.*388+1264G>T
ENST00000483148.6:c.*321G>T	ENSP00000419723.1:n.*321G>T
ENST00000485479.6:c.*415G>T	ENSP00000418144.1:n.*415G>T
ENST00000495360.6:c.*437G>T	ENSP00000419623.2:n.*437G>T
ENST00000671774.1:n.292G>T
ENST00000671912.1:c.279+1264G>T	ENSP00000500871.1:n.279+1264G>T
ENST00000672152.1:n.740+1264G>T
ENST00000672244.1:c.381+1264G>T	ENSP00000499875.1:n.381+1264G>T
ENST00000672281.1:n.891G>T
ENST00000672286.1:n.955G>T
ENST00000672438.1:c.430G>T	ENSP00000499997.1:p.Glu144Ter
ENST00000672476.1:n.886G>T
ENST00000672493.1:n.1233G>T
ENST00000672519.1:c.*388+1264G>T	ENSP00000500320.1:n.*388+1264G>T
ENST00000672535.1:c.*424G>T	ENSP00000499872.1:n.*424G>T
ENST00000672615.1:n.771G>T
ENST00000672846.1:c.*424G>T	ENSP00000500396.1:n.*424G>T
ENST00000673114.1:n.558G>T
ENST00000673171.1:n.620+1264G>T
ENST00000673211.1:n.776G>T
ENST00000673248.1:c.430G>T	ENSP00000500601.1:p.Glu144Ter
ENST00000673333.1:n.972G>T
ENST00000673360.1:c.*137G>T	ENSP00000500360.1:n.*137G>T
ENST00000673416.1:c.430G>T	ENSP00000500738.1:p.Glu144Ter
ENST00000673485.1:n.891G>T
ENST00000673487.1:c.*424G>T	ENSP00000500943.1:n.*424G>T
ENST00000673598.1:c.172G>T	ENSP00000499991.1:p.Glu58Ter
ENST00000309615.7:c.532G>T	ENSP00000311547.4:p.Glu178Ter
ENST00000379812.9:c.520G>T	ENSP00000369140.5:p.Glu174Ter
ENST00000379813.7:c.676G>T	ENSP00000369141.4:p.Glu226Ter
ENST00000379817.6:c.694G>T	ENSP00000369145.2:p.Glu232Ter
ENST00000379819.5:c.736G>T	ENSP00000369147.1:p.Glu246Ter
ENST00000379825.6:c.736G>T	ENSP00000369153.2:p.Glu246Ter
ENST00000397172.7:c.520G>T	ENSP00000380357.3:p.Glu174Ter
ENST00000436040.6:c.694G>T	ENSP00000400806.3:p.Glu232Ter
ENST00000460940.5:c.*388+1264G>T	ENSP00000418311.1:n.*388+1264G>T
ENST00000463596.5:c.694G>T	ENSP00000419846.1:p.Glu232Ter
ENST00000464632.5:c.*424G>T	ENSP00000418069.1:n.*424G>T
ENST00000465003.5:c.*321G>T	ENSP00000419430.1:n.*321G>T
ENST00000467331.5:c.*539G>T	ENSP00000418733.1:n.*539G>T
ENST00000468275.5:c.694G>T	ENSP00000420263.1:p.Glu232Ter
ENST00000472896.5:c.*273+1264G>T	ENSP00000417804.1:n.*273+1264G>T
ENST00000473221.5:c.574G>T	ENSP00000419020.1:p.Glu192Ter
ENST00000474658.6:c.361G>T
ENST00000476858.5:c.574G>T	ENSP00000419042.1:p.Glu192Ter
ENST00000478279.5:c.*321G>T	ENSP00000419597.1:n.*321G>T
ENST00000479656.5:c.*539G>T	ENSP00000420071.1:n.*539G>T
ENST00000482687.5:c.543+1264G>T	ENSP00000419289.1:n.543+1264G>T
ENST00000483148.5:c.*170+1264G>T	ENSP00000419723.1:n.*170+1264G>T
ENST00000485479.5:c.*424G>T	ENSP00000418144.1:n.*424G>T
ENST00000486724.5:n.430G>T
ENST00000494649.5:c.*539G>T	ENSP00000417634.1:n.*539G>T
ENST00000495360.5:c.*424G>T	ENSP00000419623.1:n.*424G>T
NM_001195248.1:c.736G>T	NP_001182177.1:p.Glu246Ter
NM_001195249.1:c.694G>T	NP_001182178.1:p.Glu232Ter
NM_001195250.1:c.574G>T	NP_001182179.1:p.Glu192Ter
NM_001195251.1:c.694G>T	NP_001182180.1:p.Glu232Ter
NM_001195252.1:c.520G>T	NP_001182181.1:p.Glu174Ter
NM_001195254.1:c.532G>T	NP_001182183.1:p.Glu178Ter
NM_175069.2:c.736G>T	NP_778239.1:p.Glu246Ter
NM_175073.2:c.694G>T	NP_778243.1:p.Glu232Ter
NR_036576.1:n.768G>T
NR_036577.1:n.658G>T
NR_036578.1:n.790G>T
NR_036579.1:n.937G>T
XM_006716791.2:c.694G>T	XP_006716854.1:p.Glu232Ter
XM_006716792.2:c.430G>T	XP_006716855.1:p.Glu144Ter
XM_011517936.1:c.430G>T	XP_011516238.1:p.Glu144Ter
XM_011517937.1:c.430G>T	XP_011516239.1:p.Glu144Ter
XM_011517938.1:c.430G>T	XP_011516240.1:p.Glu144Ter
XM_011517939.1:c.430G>T	XP_011516241.1:p.Glu144Ter
XR_428423.2:n.622+1264G>T
XR_929276.1:n.773G>T
XR_929277.1:n.773G>T
XR_929279.1:n.622+1264G>T
XM_006716791.4:c.694G>T	XP_006716854.1:p.Glu232Ter
XM_006716792.3:c.430G>T	XP_006716855.1:p.Glu144Ter
XM_011517938.2:c.430G>T	XP_011516240.1:p.Glu144Ter
XM_011517939.3:c.430G>T	XP_011516241.1:p.Glu144Ter
XM_017014831.1:c.736G>T	XP_016870320.1:p.Glu246Ter
XM_017014832.1:c.736G>T	XP_016870321.1:p.Glu246Ter
XM_017014833.2:c.736G>T	XP_016870322.1:p.Glu246Ter
XM_017014836.2:c.736G>T	XP_016870325.1:p.Glu246Ter
XM_017014837.2:c.532G>T	XP_016870326.1:p.Glu178Ter
XM_017014838.1:c.430G>T	XP_016870327.1:p.Glu144Ter
XM_024447575.1:c.694G>T	XP_024303343.1:p.Glu232Ter
XM_024447576.1:c.694G>T	XP_024303344.1:p.Glu232Ter
XM_024447577.1:c.694G>T	XP_024303345.1:p.Glu232Ter
XM_024447578.1:c.736G>T	XP_024303346.1:p.Glu246Ter
XM_024447579.1:c.694G>T	XP_024303347.1:p.Glu232Ter
XM_024447580.1:c.532G>T	XP_024303348.1:p.Glu178Ter
XM_024447581.1:c.430G>T	XP_024303349.1:p.Glu144Ter
XM_024447582.1:c.430G>T	XP_024303350.1:p.Glu144Ter
XR_001746325.2:n.773G>T
XR_001746326.2:n.781G>T
XR_428423.3:n.622+1264G>T
XR_929276.3:n.773G>T
XR_929277.3:n.773G>T
NM_001195248.2:c.694G>T MANE Select	NP_001182177.2:p.Glu232Ter
NM_001195250.2:c.532G>T	NP_001182179.2:p.Glu178Ter
NM_001195252.2:c.478G>T	NP_001182181.2:p.Glu160Ter
NM_001368995.1:c.694G>T	NP_001355924.1:p.Glu232Ter
NM_001368996.1:c.694G>T	NP_001355925.1:p.Glu232Ter
NM_001368997.1:c.694G>T	NP_001355926.1:p.Glu232Ter
NM_001368998.1:c.694G>T	NP_001355927.1:p.Glu232Ter
NM_001368999.1:c.694G>T	NP_001355928.1:p.Glu232Ter
NM_001369000.1:c.532G>T	NP_001355929.1:p.Glu178Ter
NM_001369001.1:c.532G>T	NP_001355930.1:p.Glu178Ter
NM_001369002.1:c.430G>T	NP_001355931.1:p.Glu144Ter
NM_001369003.1:c.430G>T	NP_001355932.1:p.Glu144Ter
NM_001369004.1:c.430G>T	NP_001355933.1:p.Glu144Ter
NM_001369005.1:c.430G>T	NP_001355934.1:p.Glu144Ter
NM_001369006.1:c.430G>T	NP_001355935.1:p.Glu144Ter
NM_001370669.1:c.430G>T	NP_001357598.1:p.Glu144Ter
NM_001370670.1:c.430G>T	NP_001357599.1:p.Glu144Ter
NM_001370673.1:c.430G>T	NP_001357602.1:p.Glu144Ter
NM_175069.3:c.694G>T	NP_778239.2:p.Glu232Ter
NR_160920.1:n.609+1264G>T
NR_160921.1:n.664G>T
NR_160922.1:n.895G>T
NR_160923.1:n.699G>T
NR_160924.1:n.704G>T
NR_160925.1:n.900G>T
NR_160926.1:n.690G>T
NR_160927.1:n.859+1264G>T
NR_160928.1:n.749+1264G>T
NR_160929.1:n.663+1264G>T
NR_160930.1:n.640G>T
NR_160931.1:n.879G>T
NM_001195249.2:c.694G>T	NP_001182178.1:p.Glu232Ter
NM_001195251.2:c.694G>T	NP_001182180.1:p.Glu232Ter
NM_001195254.2:c.532G>T	NP_001182183.1:p.Glu178Ter
NM_175073.3:c.694G>T	NP_778243.1:p.Glu232Ter
NR_036577.2:n.645G>T