Canonical Allele Identifier: CA379805065

Gene: ABCC8

Linked Data

• MyVariant Identifiers: chr11:g.17429984C>G (hg19) ; chr11:g.17408437C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17408437C>G , CM000673.2:g.17408437C>G	GRCh38
NC_000011.9:g.17429984C>G , CM000673.1:g.17429984C>G	GRCh37
NC_000011.8:g.17386560C>G	NCBI36
NG_008867.1:g.73466G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524561.2:n.2444G>C
ENST00000529967.6:n.1034G>C
ENST00000532220.2:n.507G>C
ENST00000642611.2:n.2844G>C
ENST00000682051.1:n.2791G>C
ENST00000682110.1:n.2844G>C
ENST00000682140.1:c.2772G>C	ENSP00000507829.1:p.Glu924Asp
ENST00000682185.1:n.4080G>C
ENST00000682204.1:c.*913G>C	ENSP00000507094.1:n.*913G>C
ENST00000682215.1:n.2841G>C
ENST00000682288.1:c.*1206G>C	ENSP00000507506.1:n.*1206G>C
ENST00000682442.1:n.2965G>C
ENST00000682528.1:n.2841G>C
ENST00000682673.1:n.2788G>C
ENST00000682805.1:n.2841G>C
ENST00000682965.1:c.2772G>C	ENSP00000508229.1:p.Glu924Asp
ENST00000683093.1:n.2943G>C
ENST00000683136.1:c.2772G>C	ENSP00000507768.1:p.Glu924Asp
ENST00000683153.1:n.3000G>C
ENST00000683365.1:n.2946G>C
ENST00000683377.1:n.2844G>C
ENST00000683456.1:c.2775G>C	ENSP00000508318.1:p.Glu925Asp
ENST00000683522.1:n.2844G>C
ENST00000683562.1:c.*944G>C	ENSP00000508265.1:n.*944G>C
ENST00000683693.1:n.2841G>C
ENST00000683725.1:c.2775G>C	ENSP00000507496.1:p.Glu925Asp
ENST00000684010.1:n.2759G>C
ENST00000684157.1:n.2844G>C
ENST00000684253.1:n.2747G>C
ENST00000684288.1:c.*947G>C	ENSP00000507143.1:n.*947G>C
ENST00000684313.1:n.2276G>C
ENST00000684332.1:n.2917G>C
ENST00000684371.1:n.2950G>C
ENST00000684404.1:n.2841G>C
ENST00000684442.1:n.2844G>C
ENST00000684555.1:c.*987G>C	ENSP00000507705.1:n.*987G>C
ENST00000684571.1:c.2616G>C	ENSP00000506935.1:p.Glu872Asp
ENST00000684593.1:c.*2480G>C	ENSP00000507005.1:n.*2480G>C
ENST00000684711.1:c.*1171G>C	ENSP00000506841.1:n.*1171G>C
ENST00000302539.9:c.2778G>C	ENSP00000303960.4:p.Glu926Asp
ENST00000389817.8:c.2775G>C MANE Select	ENSP00000374467.4:p.Glu925Asp
ENST00000642271.1:c.2772G>C	ENSP00000493749.1:p.Glu924Asp
ENST00000642579.1:c.859G>C
ENST00000642611.1:n.2729G>C
ENST00000642902.1:c.2610G>C
ENST00000643260.1:c.2775G>C	ENSP00000494450.1:p.Glu925Asp
ENST00000643562.1:c.*751G>C	ENSP00000496124.1:n.*751G>C
ENST00000643925.1:c.819G>C
ENST00000644447.1:c.1131G>C	ENSP00000496282.1:p.Glu377Asp
ENST00000644472.1:c.*1136G>C	ENSP00000495378.1:n.*1136G>C
ENST00000644484.1:c.*984G>C	ENSP00000493558.1:n.*984G>C
ENST00000644542.1:c.*2480G>C	ENSP00000495532.1:n.*2480G>C
ENST00000644675.1:c.*947G>C	ENSP00000494567.1:n.*947G>C
ENST00000644757.1:c.*1080G>C	ENSP00000495085.1:n.*1080G>C
ENST00000644772.1:c.2841G>C	ENSP00000494321.1:p.Glu947Asp
ENST00000645076.1:c.2027G>C
ENST00000645744.1:c.*1139G>C	ENSP00000494564.1:n.*1139G>C
ENST00000645760.1:c.3050G>C
ENST00000645884.1:c.2775G>C	ENSP00000495516.1:p.Glu925Asp
ENST00000646003.1:c.*831G>C	ENSP00000495259.1:n.*831G>C
ENST00000646207.1:c.*1139G>C	ENSP00000495025.1:n.*1139G>C
ENST00000646276.1:c.*1048G>C	ENSP00000496070.1:n.*1048G>C
ENST00000646592.1:c.2001G>C
ENST00000646902.1:c.2772G>C	ENSP00000494101.1:p.Glu924Asp
ENST00000646993.1:c.*1171G>C	ENSP00000493720.1:n.*1171G>C
ENST00000647013.1:c.2781G>C	ENSP00000496741.1:n.2781G>C
ENST00000647015.1:c.2526G>C	ENSP00000495389.1:p.Glu842Asp
ENST00000647086.1:c.*2505G>C	ENSP00000493677.1:n.*2505G>C
ENST00000647158.1:c.*916G>C	ENSP00000495744.1:n.*916G>C
ENST00000302539.8:c.2778G>C	ENSP00000303960.4:p.Glu926Asp
ENST00000389817.7:c.2775G>C	ENSP00000374467.3:p.Glu925Asp
ENST00000526921.5:n.459G>C
ENST00000527905.5:c.2745G>C	ENSP00000431653.1:p.Glu915Asp
ENST00000529967.5:n.444G>C
NM_000352.4:c.2775G>C	NP_000343.2:p.Glu925Asp
NM_001287174.1:c.2778G>C	NP_001274103.1:p.Glu926Asp
XM_011520331.1:c.2775G>C	XP_011518633.1:p.Glu925Asp
XM_011520332.1:c.2778G>C	XP_011518634.1:p.Glu926Asp
XM_011520333.1:c.1275G>C	XP_011518635.1:p.Glu425Asp
XM_011520334.1:c.2778G>C	XP_011518636.1:p.Glu926Asp
XR_930890.1:n.2841G>C
XR_930891.1:n.2841G>C
XR_930892.1:n.2841G>C
XR_930893.1:n.2838G>C
NM_001351295.1:c.2841G>C	NP_001338224.1:p.Glu947Asp
NM_001351296.1:c.2775G>C	NP_001338225.1:p.Glu925Asp
NM_001351297.1:c.2772G>C	NP_001338226.1:p.Glu924Asp
NR_147094.1:n.2844G>C
XM_017018197.2:c.2844G>C	XP_016873686.1:p.Glu948Asp
XM_017018199.1:c.2841G>C	XP_016873688.1:p.Glu947Asp
XM_017018201.2:c.2844G>C	XP_016873690.1:p.Glu948Asp
XM_017018202.1:c.1341G>C	XP_016873691.1:p.Glu447Asp
XM_017018204.1:c.732G>C	XP_016873693.1:p.Glu244Asp
XM_024448668.1:c.1143G>C	XP_024304436.1:p.Glu381Asp
XR_001747945.2:n.2916G>C
XR_001747946.2:n.2847G>C
XR_002957189.1:n.2916G>C
NM_000352.6:c.2775G>C MANE Select	NP_000343.2:p.Glu925Asp
NM_001287174.2:c.2778G>C	NP_001274103.1:p.Glu926Asp
NM_001351295.2:c.2841G>C	NP_001338224.1:p.Glu947Asp
NM_001351296.2:c.2775G>C	NP_001338225.1:p.Glu925Asp
NM_001351297.2:c.2772G>C	NP_001338226.1:p.Glu924Asp
NR_147094.2:n.2844G>C
NM_001287174.3:c.2778G>C	NP_001274103.1:p.Glu926Asp