Canonical Allele Identifier: CA1955127628
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17404656G= , CM000673.2:g.17404656G= GRCh38
NC_000011.9:g.17426203G= , CM000673.1:g.17426203G= GRCh37
NC_000011.8:g.17382779G= NCBI36
NG_008867.1:g.77247C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.2982C=
ENST00000529967.6:n.1752C=
ENST00000532220.2:n.1145C=
ENST00000642611.2:n.3482C=
ENST00000645004.2:n.912C=
ENST00000682051.1:n.3429C=
ENST00000682110.1:n.3482C=
ENST00000682140.1:c.3410C= ENSP00000507829.1:p.Thr1137=
ENST00000682185.1:n.4718C=
ENST00000682204.1:c.*1551C= ENSP00000507094.1:n.*1551C=
ENST00000682215.1:n.3479C=
ENST00000682288.1:c.*1844C= ENSP00000507506.1:n.*1844C=
ENST00000682442.1:n.3702C=
ENST00000682528.1:n.3559C=
ENST00000682673.1:n.3426C=
ENST00000682805.1:n.3479C=
ENST00000682965.1:c.3396+838C= ENSP00000508229.1:n.3396+838C=
ENST00000683093.1:n.3581C=
ENST00000683136.1:c.3410C= ENSP00000507768.1:p.Thr1137=
ENST00000683153.1:n.3638C=
ENST00000683365.1:n.3584C=
ENST00000683377.1:n.3482C=
ENST00000683456.1:c.*550C= ENSP00000508318.1:n.*550C=
ENST00000683522.1:n.3482C=
ENST00000683562.1:c.*1582C= ENSP00000508265.1:n.*1582C=
ENST00000683693.1:n.3559C=
ENST00000683725.1:c.3413C= ENSP00000507496.1:p.Thr1138=
ENST00000684010.1:n.3477C=
ENST00000684157.1:n.3482C=
ENST00000684253.1:n.3385C=
ENST00000684288.1:c.*1585C= ENSP00000507143.1:n.*1585C=
ENST00000684313.1:n.2914C=
ENST00000684332.1:n.3555C=
ENST00000684371.1:n.3588C=
ENST00000684404.1:n.3525C=
ENST00000684442.1:n.3482C=
ENST00000684555.1:c.*1625C= ENSP00000507705.1:n.*1625C=
ENST00000684571.1:c.3254C= ENSP00000506935.1:p.Thr1085=
ENST00000684593.1:c.*3118C= ENSP00000507005.1:n.*3118C=
ENST00000684711.1:c.*1809C= ENSP00000506841.1:n.*1809C=
ENST00000302539.9:c.3416C= ENSP00000303960.4:p.Thr1139=
ENST00000389817.8:c.3413C= MANE Select ENSP00000374467.4:p.Thr1138=
ENST00000642271.1:c.3410C= ENSP00000493749.1:p.Thr1137=
ENST00000642579.1:c.1497C=
ENST00000642611.1:n.3367C=
ENST00000642902.1:c.3195C=
ENST00000643260.1:c.3413C= ENSP00000494450.1:p.Thr1138=
ENST00000643562.1:c.*1389C= ENSP00000496124.1:n.*1389C=
ENST00000643925.1:c.1537C=
ENST00000644447.1:c.1769C= ENSP00000496282.1:p.Thr590=
ENST00000644484.1:c.*1668C= ENSP00000493558.1:n.*1668C=
ENST00000644675.1:c.*1585C= ENSP00000494567.1:n.*1585C=
ENST00000644757.1:c.*1698C= ENSP00000495085.1:n.*1698C=
ENST00000644772.1:c.3479C= ENSP00000494321.1:p.Thr1160=
ENST00000645004.1:n.552C=
ENST00000645076.1:c.2612C=
ENST00000645417.1:c.579C=
ENST00000645744.1:c.*1677C= ENSP00000494564.1:n.*1677C=
ENST00000645760.1:c.3688C=
ENST00000645884.1:c.*550C= ENSP00000495516.1:n.*550C=
ENST00000646003.1:c.*1369C= ENSP00000495259.1:n.*1369C=
ENST00000646207.1:c.*1880C= ENSP00000495025.1:n.*1880C=
ENST00000646276.1:c.*1686C= ENSP00000496070.1:n.*1686C=
ENST00000646592.1:c.2719C=
ENST00000646902.1:c.3410C= ENSP00000494101.1:p.Thr1137=
ENST00000646993.1:c.*1809C= ENSP00000493720.1:n.*1809C=
ENST00000647013.1:c.3419C= ENSP00000496741.1:n.3419C=
ENST00000647015.1:c.3164C= ENSP00000495389.1:p.Thr1055=
ENST00000647086.1:c.*3143C= ENSP00000493677.1:n.*3143C=
ENST00000647158.1:c.*1554C= ENSP00000495744.1:n.*1554C=
ENST00000302539.8:c.3416C= ENSP00000303960.4:p.Thr1139=
ENST00000389817.7:c.3413C= ENSP00000374467.3:p.Thr1138=
ENST00000524561.1:n.545C=
ENST00000527905.5:c.*289C= ENSP00000431653.1:n.*289C=
NM_000352.4:c.3413C= NP_000343.2:p.Thr1138=
NM_001287174.1:c.3416C= NP_001274103.1:p.Thr1139=
XM_011520331.1:c.3413C= XP_011518633.1:p.Thr1138=
XM_011520332.1:c.3416C= XP_011518634.1:p.Thr1139=
XM_011520333.1:c.1913C= XP_011518635.1:p.Thr638=
XR_930890.1:n.3479C=
XR_930891.1:n.3480C=
XR_930892.1:n.3379C=
XR_930893.1:n.3376C=
NM_001351295.1:c.3479C= NP_001338224.1:p.Thr1160=
NM_001351296.1:c.3413C= NP_001338225.1:p.Thr1138=
NM_001351297.1:c.3410C= NP_001338226.1:p.Thr1137=
NR_147094.1:n.3562C=
XM_017018197.2:c.3482C= XP_016873686.1:p.Thr1161=
XM_017018199.1:c.3479C= XP_016873688.1:p.Thr1160=
XM_017018201.2:c.3482C= XP_016873690.1:p.Thr1161=
XM_017018202.1:c.1979C= XP_016873691.1:p.Thr660=
XM_017018204.1:c.1370C= XP_016873693.1:p.Thr457=
XM_024448668.1:c.1781C= XP_024304436.1:p.Thr594=
XR_001747945.2:n.3554C=
XR_001747946.2:n.3485C=
XR_002957189.1:n.3634C=
NM_000352.6:c.3413C= MANE Select NP_000343.2:p.Thr1138=
NM_001287174.2:c.3416C= NP_001274103.1:p.Thr1139=
NM_001351295.2:c.3479C= NP_001338224.1:p.Thr1160=
NM_001351296.2:c.3413C= NP_001338225.1:p.Thr1138=
NM_001351297.2:c.3410C= NP_001338226.1:p.Thr1137=
NR_147094.2:n.3562C=
NM_001287174.3:c.3416C= NP_001274103.1:p.Thr1139=