Canonical Allele Identifier: CA2473712619
Gene: MUTYH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45332228T= , CM000663.2:g.45332228T= GRCh38
NC_000001.10:g.45797900T= , CM000663.1:g.45797900T= GRCh37
NC_000001.9:g.45570487T= NCBI36
NG_008189.1:g.13243A= , LRG_220:g.13243A=

Transcript Alleles

HGVS Amino-acid change
ENST00000412971.6:c.403A= ENSP00000410263.2:p.Thr135=
ENST00000435155.2:c.820A= ENSP00000403655.2:p.Thr274=
ENST00000467459.6:c.787A= ENSP00000435889.2:p.Thr263=
ENST00000483127.2:c.805A= ENSP00000436469.2:p.Thr269=
ENST00000485271.6:c.787A= ENSP00000431264.2:p.Thr263=
ENST00000529892.6:c.829A= ENSP00000432528.2:p.Thr277=
ENST00000533178.6:c.*116A= ENSP00000436430.2:n.*116A=
ENST00000672314.2:c.787A= ENSP00000500828.2:p.Thr263=
ENST00000674679.2:c.*699A= ENSP00000501623.2:n.*699A=
ENST00000710952.2:c.871A= MANE Plus Clinical ENSP00000518552.2:p.Thr291=
ENST00000672818.3:c.862A= ENSP00000500891.1:p.Thr288=
ENST00000450313.6:c.*116A= ENSP00000408176.2:n.*116A=
ENST00000456914.7:c.787A= MANE Select ENSP00000407590.2:p.Thr263=
ENST00000461495.6:c.*526A= ENSP00000437166.1:n.*526A=
ENST00000671898.1:c.1375A= ENSP00000499896.1:p.Thr459=
ENST00000672011.1:c.*116A= ENSP00000500418.1:n.*116A=
ENST00000672314.1:c.787A= ENSP00000500828.1:p.Thr263=
ENST00000672593.1:c.*840A= ENSP00000500455.1:n.*840A=
ENST00000672764.1:c.*116A= ENSP00000500886.1:n.*116A=
ENST00000672818.2:c.862A= ENSP00000500891.1:p.Thr288=
ENST00000673134.1:c.*484A= ENSP00000500526.1:n.*484A=
ENST00000674679.1:c.815A= ENSP00000501623.1:n.815A=
ENST00000354383.10:c.790A= ENSP00000346354.6:p.Thr264=
ENST00000355498.6:c.787A= ENSP00000347685.2:p.Thr263=
ENST00000372098.7:c.862A= ENSP00000361170.3:p.Thr288=
ENST00000372104.5:c.787A= ENSP00000361176.1:p.Thr263=
ENST00000372110.7:c.832A= ENSP00000361182.3:p.Thr278=
ENST00000372115.7:c.829A= ENSP00000361187.3:p.Thr277=
ENST00000412971.5:c.403A= ENSP00000410263.1:p.Thr135=
ENST00000435155.1:c.820A= ENSP00000403655.1:p.Thr274=
ENST00000448481.5:c.820A= ENSP00000409718.1:p.Thr274=
ENST00000450313.5:c.871A= ENSP00000408176.1:p.Thr291=
ENST00000456914.6:c.787A= ENSP00000407590.2:p.Thr263=
ENST00000461495.5:c.*526A= ENSP00000437166.1:n.*526A=
ENST00000462388.5:n.478A=
ENST00000466231.1:n.152A=
ENST00000467459.5:c.181A= ENSP00000435889.1:p.Thr61=
ENST00000467940.5:c.*710A= ENSP00000436478.1:n.*710A=
ENST00000470256.5:c.*116A= ENSP00000434985.1:n.*116A=
ENST00000475516.5:c.*600A= ENSP00000433843.1:n.*600A=
ENST00000478796.5:n.774A=
ENST00000481571.5:c.*600A= ENSP00000436597.1:n.*600A=
ENST00000488731.6:c.187+535A= ENSP00000432330.1:n.187+535A=
ENST00000528013.6:c.829A= ENSP00000433130.2:p.Thr277=
ENST00000529892.5:c.51A=
ENST00000529984.5:c.187+535A= ENSP00000437093.1:n.187+535A=
ENST00000531105.5:c.115+2163A= ENSP00000431292.1:n.115+2163A=
ENST00000533178.5:c.416A= ENSP00000436430.1:n.416A=
NM_001048171.1:c.829A= NP_001041636.1:p.Thr277=
NM_001048172.1:c.790A= NP_001041637.1:p.Thr264=
NM_001048173.1:c.787A= NP_001041638.1:p.Thr263=
NM_001048174.1:c.787A= NP_001041639.1:p.Thr263=
NM_001128425.1:c.871A= , LRG_220t1:c.871A= NP_001121897.1:p.Thr291=
NM_001293190.1:c.832A= NP_001280119.1:p.Thr278=
NM_001293191.1:c.820A= NP_001280120.1:p.Thr274=
NM_001293192.1:c.511A= NP_001280121.1:p.Thr171=
NM_001293195.1:c.787A= NP_001280124.1:p.Thr263=
NM_001293196.1:c.511A= NP_001280125.1:p.Thr171=
NM_012222.2:c.862A= NP_036354.1:p.Thr288=
XM_011541497.1:c.847A= XP_011539799.1:p.Thr283=
XM_011541498.1:c.829A= XP_011539800.1:p.Thr277=
XM_011541499.1:c.829A= XP_011539801.1:p.Thr277=
XM_011541500.1:c.829A= XP_011539802.1:p.Thr277=
XM_011541501.1:c.829A= XP_011539803.1:p.Thr277=
XM_011541502.1:c.829A= XP_011539804.1:p.Thr277=
XM_011541503.1:c.829A= XP_011539805.1:p.Thr277=
XM_011541504.1:c.820A= XP_011539806.1:p.Thr274=
XM_011541505.1:c.409A= XP_011539807.1:p.Thr137=
XM_011541506.1:c.409A= XP_011539808.1:p.Thr137=
XM_011541507.1:c.400A= XP_011539809.1:p.Thr134=
XM_011541508.1:c.415A= XP_011539810.1:p.Thr139=
XR_946658.1:n.918A=
NM_001350650.1:c.442A= NP_001337579.1:p.Thr148=
NM_001350651.1:c.442A= NP_001337580.1:p.Thr148=
NR_146882.1:n.1045A=
NR_146883.1:n.859A=
XM_011541497.3:c.847A= XP_011539799.1:p.Thr283=
XM_011541500.3:c.829A= XP_011539802.1:p.Thr277=
XM_011541501.2:c.829A= XP_011539803.1:p.Thr277=
XM_011541502.2:c.829A= XP_011539804.1:p.Thr277=
XM_011541503.2:c.829A= XP_011539805.1:p.Thr277=
XM_011541504.2:c.820A= XP_011539806.1:p.Thr274=
XM_011541505.2:c.409A= XP_011539807.1:p.Thr137=
XM_011541506.2:c.409A= XP_011539808.1:p.Thr137=
XM_017001331.1:c.829A= XP_016856820.1:p.Thr277=
XM_017001332.1:c.829A= XP_016856821.1:p.Thr277=
XM_017001333.1:c.829A= XP_016856822.1:p.Thr277=
XM_017001334.1:c.790A= XP_016856823.1:p.Thr264=
XM_017001335.1:c.511A= XP_016856824.1:p.Thr171=
XM_017001336.1:c.442A= XP_016856825.1:p.Thr148=
XM_017001337.1:c.442A= XP_016856826.1:p.Thr148=
XM_024447244.1:c.442A= XP_024303012.1:p.Thr148=
XM_024447245.1:c.442A= XP_024303013.1:p.Thr148=
XM_024447248.1:c.400A= XP_024303016.1:p.Thr134=
XM_024447249.1:c.271A= XP_024303017.1:p.Thr91=
XM_024447250.1:c.271A= XP_024303018.1:p.Thr91=
XM_024447251.1:c.271A= XP_024303019.1:p.Thr91=
XR_001737190.1:n.832A=
XR_001737192.1:n.644A=
XR_002956643.1:n.824A=
XR_002956644.1:n.1359A=
XR_946658.2:n.932A=
NM_001048171.2:c.787A= NP_001041636.2:p.Thr263=
NM_001128425.2:c.871A= MANE Plus Clinical NP_001121897.1:p.Thr291=
NM_001048172.2:c.790A= NP_001041637.1:p.Thr264=
NM_001048173.2:c.787A= NP_001041638.1:p.Thr263=
NM_001048174.2:c.787A= MANE Select NP_001041639.1:p.Thr263=
NM_001293190.2:c.832A= NP_001280119.1:p.Thr278=
NM_001293191.2:c.820A= NP_001280120.1:p.Thr274=
NM_001293192.2:c.511A= NP_001280121.1:p.Thr171=
NM_001293195.2:c.787A= NP_001280124.1:p.Thr263=
NM_001293196.2:c.511A= NP_001280125.1:p.Thr171=
NM_001350650.2:c.442A= NP_001337579.1:p.Thr148=
NM_001350651.2:c.442A= NP_001337580.1:p.Thr148=
NM_012222.3:c.862A= NP_036354.1:p.Thr288=
NR_146882.2:n.1015A=
NR_146883.2:n.864A=