Canonical Allele Identifier: CA1955131320
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17412678G= , CM000673.2:g.17412678G= GRCh38
NC_000011.9:g.17434225G= , CM000673.1:g.17434225G= GRCh37
NC_000011.8:g.17390801G= NCBI36
NG_008867.1:g.69225C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.2213C=
ENST00000529967.6:n.803C=
ENST00000642611.2:n.2613C=
ENST00000682051.1:n.2560C=
ENST00000682110.1:n.2613C=
ENST00000682140.1:c.2541C= ENSP00000507829.1:p.Asn847=
ENST00000682185.1:n.3849C=
ENST00000682204.1:c.*682C= ENSP00000507094.1:n.*682C=
ENST00000682215.1:n.2610C=
ENST00000682288.1:c.*975C= ENSP00000507506.1:n.*975C=
ENST00000682442.1:n.2734C=
ENST00000682528.1:n.2610C=
ENST00000682673.1:n.2557C=
ENST00000682805.1:n.2610C=
ENST00000682965.1:c.2541C= ENSP00000508229.1:p.Asn847=
ENST00000683093.1:n.2712C=
ENST00000683136.1:c.2541C= ENSP00000507768.1:p.Asn847=
ENST00000683153.1:n.2769C=
ENST00000683365.1:n.2715C=
ENST00000683377.1:n.2613C=
ENST00000683456.1:c.2544C= ENSP00000508318.1:p.Asn848=
ENST00000683522.1:n.2613C=
ENST00000683562.1:c.*713C= ENSP00000508265.1:n.*713C=
ENST00000683693.1:n.2610C=
ENST00000683725.1:c.2544C= ENSP00000507496.1:p.Asn848=
ENST00000684010.1:n.2528C=
ENST00000684157.1:n.2613C=
ENST00000684253.1:n.2516C=
ENST00000684288.1:c.*716C= ENSP00000507143.1:n.*716C=
ENST00000684313.1:n.2045C=
ENST00000684332.1:n.2686C=
ENST00000684371.1:n.2719C=
ENST00000684404.1:n.2610C=
ENST00000684442.1:n.2613C=
ENST00000684555.1:c.*756C= ENSP00000507705.1:n.*756C=
ENST00000684571.1:c.2385C= ENSP00000506935.1:p.Asn795=
ENST00000684593.1:c.*2249C= ENSP00000507005.1:n.*2249C=
ENST00000684711.1:c.*940C= ENSP00000506841.1:n.*940C=
ENST00000302539.9:c.2547C= ENSP00000303960.4:p.Asn849=
ENST00000389817.8:c.2544C= MANE Select ENSP00000374467.4:p.Asn848=
ENST00000642271.1:c.2541C= ENSP00000493749.1:p.Asn847=
ENST00000642579.1:c.628C=
ENST00000642611.1:n.2498C=
ENST00000642902.1:c.2379C=
ENST00000643260.1:c.2544C= ENSP00000494450.1:p.Asn848=
ENST00000643562.1:c.*520C= ENSP00000496124.1:n.*520C=
ENST00000643925.1:c.588C=
ENST00000644447.1:c.900C= ENSP00000496282.1:p.Asn300=
ENST00000644472.1:c.*905C= ENSP00000495378.1:n.*905C=
ENST00000644484.1:c.*753C= ENSP00000493558.1:n.*753C=
ENST00000644542.1:c.*2249C= ENSP00000495532.1:n.*2249C=
ENST00000644675.1:c.*716C= ENSP00000494567.1:n.*716C=
ENST00000644757.1:c.*849C= ENSP00000495085.1:n.*849C=
ENST00000644772.1:c.2610C= ENSP00000494321.1:p.Asn870=
ENST00000645076.1:c.1796C=
ENST00000645744.1:c.*908C= ENSP00000494564.1:n.*908C=
ENST00000645760.1:c.2819C=
ENST00000645884.1:c.2544C= ENSP00000495516.1:p.Asn848=
ENST00000646003.1:c.*600C= ENSP00000495259.1:n.*600C=
ENST00000646207.1:c.*908C= ENSP00000495025.1:n.*908C=
ENST00000646276.1:c.*817C= ENSP00000496070.1:n.*817C=
ENST00000646592.1:c.1770C=
ENST00000646902.1:c.2541C= ENSP00000494101.1:p.Asn847=
ENST00000646993.1:c.*940C= ENSP00000493720.1:n.*940C=
ENST00000647013.1:c.2550C= ENSP00000496741.1:n.2550C=
ENST00000647015.1:c.2295C= ENSP00000495389.1:p.Asn765=
ENST00000647086.1:c.*2274C= ENSP00000493677.1:n.*2274C=
ENST00000647158.1:c.*685C= ENSP00000495744.1:n.*685C=
ENST00000302539.8:c.2547C= ENSP00000303960.4:p.Asn849=
ENST00000389817.7:c.2544C= ENSP00000374467.3:p.Asn848=
ENST00000526921.5:n.228C=
ENST00000527905.5:c.2514C= ENSP00000431653.1:p.Asn838=
ENST00000529967.5:n.213C=
ENST00000530147.5:n.127C=
ENST00000531911.1:n.658C=
NM_000352.4:c.2544C= NP_000343.2:p.Asn848=
NM_001287174.1:c.2547C= NP_001274103.1:p.Asn849=
XM_011520331.1:c.2544C= XP_011518633.1:p.Asn848=
XM_011520332.1:c.2547C= XP_011518634.1:p.Asn849=
XM_011520333.1:c.1044C= XP_011518635.1:p.Asn348=
XM_011520334.1:c.2547C= XP_011518636.1:p.Asn849=
XR_930890.1:n.2610C=
XR_930891.1:n.2610C=
XR_930892.1:n.2610C=
XR_930893.1:n.2607C=
NM_001351295.1:c.2610C= NP_001338224.1:p.Asn870=
NM_001351296.1:c.2544C= NP_001338225.1:p.Asn848=
NM_001351297.1:c.2541C= NP_001338226.1:p.Asn847=
NR_147094.1:n.2613C=
XM_017018197.2:c.2613C= XP_016873686.1:p.Asn871=
XM_017018199.1:c.2610C= XP_016873688.1:p.Asn870=
XM_017018201.2:c.2613C= XP_016873690.1:p.Asn871=
XM_017018202.1:c.1110C= XP_016873691.1:p.Asn370=
XM_017018204.1:c.501C= XP_016873693.1:p.Asn167=
XM_024448668.1:c.912C= XP_024304436.1:p.Asn304=
XR_001747945.2:n.2685C=
XR_001747946.2:n.2616C=
XR_002957189.1:n.2685C=
NM_000352.6:c.2544C= MANE Select NP_000343.2:p.Asn848=
NM_001287174.2:c.2547C= NP_001274103.1:p.Asn849=
NM_001351295.2:c.2610C= NP_001338224.1:p.Asn870=
NM_001351296.2:c.2544C= NP_001338225.1:p.Asn848=
NM_001351297.2:c.2541C= NP_001338226.1:p.Asn847=
NR_147094.2:n.2613C=
NM_001287174.3:c.2547C= NP_001274103.1:p.Asn849=