Canonical Allele Identifier: CA1955127623
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17404640G= , CM000673.2:g.17404640G= GRCh38
NC_000011.9:g.17426187G= , CM000673.1:g.17426187G= GRCh37
NC_000011.8:g.17382763G= NCBI36
NG_008867.1:g.77263C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.2998C=
ENST00000528374.2:c.8C=
ENST00000529967.6:n.1768C=
ENST00000532220.2:n.1161C=
ENST00000642611.2:n.3498C=
ENST00000645004.2:n.928C=
ENST00000682051.1:n.3445C=
ENST00000682110.1:n.3498C=
ENST00000682140.1:c.3426C= ENSP00000507829.1:p.Ser1142=
ENST00000682185.1:n.4734C=
ENST00000682204.1:c.*1567C= ENSP00000507094.1:n.*1567C=
ENST00000682215.1:n.3495C=
ENST00000682288.1:c.*1860C= ENSP00000507506.1:n.*1860C=
ENST00000682442.1:n.3718C=
ENST00000682528.1:n.3575C=
ENST00000682673.1:n.3442C=
ENST00000682805.1:n.3495C=
ENST00000682965.1:c.3396+854C= ENSP00000508229.1:n.3396+854C=
ENST00000683093.1:n.3597C=
ENST00000683136.1:c.3426C= ENSP00000507768.1:p.Ser1142=
ENST00000683153.1:n.3654C=
ENST00000683365.1:n.3600C=
ENST00000683377.1:n.3498C=
ENST00000683456.1:c.*566C= ENSP00000508318.1:n.*566C=
ENST00000683522.1:n.3498C=
ENST00000683562.1:c.*1598C= ENSP00000508265.1:n.*1598C=
ENST00000683693.1:n.3575C=
ENST00000683725.1:c.3429C= ENSP00000507496.1:p.Ser1143=
ENST00000684010.1:n.3493C=
ENST00000684157.1:n.3498C=
ENST00000684253.1:n.3401C=
ENST00000684288.1:c.*1601C= ENSP00000507143.1:n.*1601C=
ENST00000684313.1:n.2930C=
ENST00000684332.1:n.3571C=
ENST00000684371.1:n.3604C=
ENST00000684404.1:n.3541C=
ENST00000684442.1:n.3498C=
ENST00000684555.1:c.*1641C= ENSP00000507705.1:n.*1641C=
ENST00000684571.1:c.3270C= ENSP00000506935.1:p.Ser1090=
ENST00000684593.1:c.*3134C= ENSP00000507005.1:n.*3134C=
ENST00000684711.1:c.*1825C= ENSP00000506841.1:n.*1825C=
ENST00000302539.9:c.3432C= ENSP00000303960.4:p.Ser1144=
ENST00000389817.8:c.3429C= MANE Select ENSP00000374467.4:p.Ser1143=
ENST00000642271.1:c.3426C= ENSP00000493749.1:p.Ser1142=
ENST00000642579.1:c.1513C=
ENST00000642611.1:n.3383C=
ENST00000642902.1:c.3211C=
ENST00000643260.1:c.3429C= ENSP00000494450.1:p.Ser1143=
ENST00000643562.1:c.*1405C= ENSP00000496124.1:n.*1405C=
ENST00000643925.1:c.1553C=
ENST00000644447.1:c.1785C= ENSP00000496282.1:p.Ser595=
ENST00000644484.1:c.*1684C= ENSP00000493558.1:n.*1684C=
ENST00000644675.1:c.*1601C= ENSP00000494567.1:n.*1601C=
ENST00000644757.1:c.*1714C= ENSP00000495085.1:n.*1714C=
ENST00000644772.1:c.3495C= ENSP00000494321.1:p.Ser1165=
ENST00000645004.1:n.568C=
ENST00000645076.1:c.2628C=
ENST00000645417.1:c.595C=
ENST00000645744.1:c.*1693C= ENSP00000494564.1:n.*1693C=
ENST00000645760.1:c.3704C=
ENST00000645884.1:c.*566C= ENSP00000495516.1:n.*566C=
ENST00000646003.1:c.*1385C= ENSP00000495259.1:n.*1385C=
ENST00000646207.1:c.*1896C= ENSP00000495025.1:n.*1896C=
ENST00000646276.1:c.*1702C= ENSP00000496070.1:n.*1702C=
ENST00000646592.1:c.2735C=
ENST00000646902.1:c.3426C= ENSP00000494101.1:p.Ser1142=
ENST00000646993.1:c.*1825C= ENSP00000493720.1:n.*1825C=
ENST00000647013.1:c.3435C= ENSP00000496741.1:n.3435C=
ENST00000647015.1:c.3180C= ENSP00000495389.1:p.Ser1060=
ENST00000647086.1:c.*3159C= ENSP00000493677.1:n.*3159C=
ENST00000647158.1:c.*1570C= ENSP00000495744.1:n.*1570C=
ENST00000302539.8:c.3432C= ENSP00000303960.4:p.Ser1144=
ENST00000389817.7:c.3429C= ENSP00000374467.3:p.Ser1143=
ENST00000524561.1:n.561C=
ENST00000527905.5:c.*305C= ENSP00000431653.1:n.*305C=
NM_000352.4:c.3429C= NP_000343.2:p.Ser1143=
NM_001287174.1:c.3432C= NP_001274103.1:p.Ser1144=
XM_011520331.1:c.3429C= XP_011518633.1:p.Ser1143=
XM_011520332.1:c.3432C= XP_011518634.1:p.Ser1144=
XM_011520333.1:c.1929C= XP_011518635.1:p.Ser643=
XR_930890.1:n.3495C=
XR_930892.1:n.3395C=
XR_930893.1:n.3392C=
NM_001351295.1:c.3495C= NP_001338224.1:p.Ser1165=
NM_001351296.1:c.3429C= NP_001338225.1:p.Ser1143=
NM_001351297.1:c.3426C= NP_001338226.1:p.Ser1142=
NR_147094.1:n.3578C=
XM_017018197.2:c.3498C= XP_016873686.1:p.Ser1166=
XM_017018199.1:c.3495C= XP_016873688.1:p.Ser1165=
XM_017018201.2:c.3498C= XP_016873690.1:p.Ser1166=
XM_017018202.1:c.1995C= XP_016873691.1:p.Ser665=
XM_017018204.1:c.1386C= XP_016873693.1:p.Ser462=
XM_024448668.1:c.1797C= XP_024304436.1:p.Ser599=
XR_001747945.2:n.3570C=
XR_001747946.2:n.3501C=
XR_002957189.1:n.3650C=
NM_000352.6:c.3429C= MANE Select NP_000343.2:p.Ser1143=
NM_001287174.2:c.3432C= NP_001274103.1:p.Ser1144=
NM_001351295.2:c.3495C= NP_001338224.1:p.Ser1165=
NM_001351296.2:c.3429C= NP_001338225.1:p.Ser1143=
NM_001351297.2:c.3426C= NP_001338226.1:p.Ser1142=
NR_147094.2:n.3578C=
NM_001287174.3:c.3432C= NP_001274103.1:p.Ser1144=