Canonical Allele Identifier: CA1955122290
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17393698G= , CM000673.2:g.17393698G= GRCh38
NC_000011.9:g.17415245G= , CM000673.1:g.17415245G= GRCh37
NC_000011.8:g.17371821G= NCBI36
NG_008867.1:g.88205C=

Transcript Alleles

HGVS Amino-acid change
ENST00000524561.2:n.4208C=
ENST00000526037.6:n.542C=
ENST00000528374.2:c.1198C=
ENST00000529967.6:n.2946C=
ENST00000532220.2:n.3840C=
ENST00000642611.2:n.5940C=
ENST00000644057.2:n.1183C=
ENST00000645004.2:n.2106C=
ENST00000682051.1:n.4769C=
ENST00000682110.1:n.4822C=
ENST00000682140.1:c.*393C= ENSP00000507829.1:n.*393C=
ENST00000682185.1:n.5912C=
ENST00000682204.1:c.*2745C= ENSP00000507094.1:n.*2745C=
ENST00000682215.1:n.5189C=
ENST00000682288.1:c.*3038C= ENSP00000507506.1:n.*3038C=
ENST00000682442.1:n.5042C=
ENST00000682528.1:n.4899C=
ENST00000682673.1:n.4766C=
ENST00000682805.1:n.5227C=
ENST00000682965.1:c.*1029C= ENSP00000508229.1:n.*1029C=
ENST00000683093.1:n.5802C=
ENST00000683136.1:c.4490C= ENSP00000507768.1:p.Ala1497=
ENST00000683153.1:n.4864C=
ENST00000683365.1:n.4924C=
ENST00000683377.1:n.4718C=
ENST00000683456.1:c.*1744C= ENSP00000508318.1:n.*1744C=
ENST00000683522.1:n.4904C=
ENST00000683562.1:c.*2672C= ENSP00000508265.1:n.*2672C=
ENST00000683693.1:n.6283C=
ENST00000683725.1:c.*72C= ENSP00000507496.1:n.*72C=
ENST00000684010.1:n.4817C=
ENST00000684014.1:n.794C=
ENST00000684157.1:n.5807C=
ENST00000684253.1:n.4725C=
ENST00000684288.1:c.*2779C= ENSP00000507143.1:n.*2779C=
ENST00000684313.1:n.4254C=
ENST00000684332.1:n.4895C=
ENST00000684371.1:n.4928C=
ENST00000684404.1:n.5850C=
ENST00000684442.1:n.5046C=
ENST00000684555.1:c.*2819C= ENSP00000507705.1:n.*2819C=
ENST00000684571.1:c.4448C= ENSP00000506935.1:p.Ala1483=
ENST00000684593.1:c.*4312C= ENSP00000507005.1:n.*4312C=
ENST00000684711.1:c.*3003C= ENSP00000506841.1:n.*3003C=
ENST00000302539.9:c.4610C= ENSP00000303960.4:p.Ala1537=
ENST00000389817.8:c.4607C= MANE Select ENSP00000374467.4:p.Ala1536=
ENST00000642271.1:c.4604C= ENSP00000493749.1:p.Ala1535=
ENST00000642579.1:c.2661C=
ENST00000642611.1:n.5825C=
ENST00000642902.1:c.4389C=
ENST00000643260.1:c.4607C= ENSP00000494450.1:p.Ala1536=
ENST00000643562.1:c.*2729C= ENSP00000496124.1:n.*2729C=
ENST00000643925.1:c.3185+568C=
ENST00000644057.1:n.766C=
ENST00000644484.1:c.*3993C= ENSP00000493558.1:n.*3993C=
ENST00000644675.1:c.*2779C= ENSP00000494567.1:n.*2779C=
ENST00000644757.1:c.*3203-718C= ENSP00000495085.1:n.*3203-718C=
ENST00000644772.1:c.4673C= ENSP00000494321.1:p.Ala1558=
ENST00000645004.1:n.2300C=
ENST00000645076.1:c.3702C=
ENST00000645417.1:c.1795C=
ENST00000645744.1:c.*4292C= ENSP00000494564.1:n.*4292C=
ENST00000645760.1:c.5028C=
ENST00000645884.1:c.*1890C= ENSP00000495516.1:n.*1890C=
ENST00000646003.1:c.*2629C= ENSP00000495259.1:n.*2629C=
ENST00000646207.1:c.*3444C= ENSP00000495025.1:n.*3444C=
ENST00000646276.1:c.*4011C= ENSP00000496070.1:n.*4011C=
ENST00000646592.1:c.3913C=
ENST00000646902.1:c.4574C= ENSP00000494101.1:p.Ala1525=
ENST00000646993.1:c.*3045C= ENSP00000493720.1:n.*3045C=
ENST00000647015.1:c.4358C= ENSP00000495389.1:p.Ala1453=
ENST00000647086.1:c.*4193C= ENSP00000493677.1:n.*4193C=
ENST00000647158.1:c.*2894C= ENSP00000495744.1:n.*2894C=
ENST00000302539.8:c.4610C= ENSP00000303960.4:p.Ala1537=
ENST00000389817.7:c.4607C= ENSP00000374467.3:p.Ala1536=
ENST00000525022.1:n.502C=
ENST00000526037.5:n.367C=
ENST00000526168.5:c.395C=
ENST00000531642.5:c.638C=
NM_000352.4:c.4607C= NP_000343.2:p.Ala1536=
NM_001287174.1:c.4610C= NP_001274103.1:p.Ala1537=
XM_011520331.1:c.4607C= XP_011518633.1:p.Ala1536=
XM_011520333.1:c.3107C= XP_011518635.1:p.Ala1036=
XR_930890.1:n.4569C=
NM_001351295.1:c.4673C= NP_001338224.1:p.Ala1558=
NM_001351296.1:c.4607C= NP_001338225.1:p.Ala1536=
NM_001351297.1:c.4604C= NP_001338226.1:p.Ala1535=
NR_147094.1:n.4902C=
XM_017018197.2:c.4676C= XP_016873686.1:p.Ala1559=
XM_017018199.1:c.4673C= XP_016873688.1:p.Ala1558=
XM_017018202.1:c.3173C= XP_016873691.1:p.Ala1058=
XM_017018204.1:c.2564C= XP_016873693.1:p.Ala855=
XM_024448668.1:c.2975C= XP_024304436.1:p.Ala992=
XR_001747945.2:n.4644C=
XR_001747946.2:n.4575C=
XR_002957189.1:n.6358C=
NM_000352.6:c.4607C= MANE Select NP_000343.2:p.Ala1536=
NM_001287174.2:c.4610C= NP_001274103.1:p.Ala1537=
NM_001351295.2:c.4673C= NP_001338224.1:p.Ala1558=
NM_001351296.2:c.4607C= NP_001338225.1:p.Ala1536=
NM_001351297.2:c.4604C= NP_001338226.1:p.Ala1535=
NR_147094.2:n.4902C=
NM_001287174.3:c.4610C= NP_001274103.1:p.Ala1537=