Canonical Allele Identifier: CA1955127586
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17404574C= , CM000673.2:g.17404574C= GRCh38
NC_000011.9:g.17426121C= , CM000673.1:g.17426121C= GRCh37
NC_000011.8:g.17382697C= NCBI36
NG_008867.1:g.77329G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.3064G=
ENST00000528374.2:c.74G=
ENST00000529967.6:n.1834G=
ENST00000532220.2:n.1227G=
ENST00000642611.2:n.3564G=
ENST00000645004.2:n.994G=
ENST00000682051.1:n.3511G=
ENST00000682110.1:n.3564G=
ENST00000682140.1:c.3492G= ENSP00000507829.1:p.Val1164=
ENST00000682185.1:n.4800G=
ENST00000682204.1:c.*1633G= ENSP00000507094.1:n.*1633G=
ENST00000682215.1:n.3561G=
ENST00000682288.1:c.*1926G= ENSP00000507506.1:n.*1926G=
ENST00000682442.1:n.3784G=
ENST00000682528.1:n.3641G=
ENST00000682673.1:n.3508G=
ENST00000682805.1:n.3561G=
ENST00000682965.1:c.3396+920G= ENSP00000508229.1:n.3396+920G=
ENST00000683093.1:n.3663G=
ENST00000683136.1:c.3492G= ENSP00000507768.1:p.Val1164=
ENST00000683153.1:n.3720G=
ENST00000683365.1:n.3666G=
ENST00000683377.1:n.3564G=
ENST00000683456.1:c.*632G= ENSP00000508318.1:n.*632G=
ENST00000683522.1:n.3564G=
ENST00000683562.1:c.*1664G= ENSP00000508265.1:n.*1664G=
ENST00000683693.1:n.3641G=
ENST00000683725.1:c.3495G= ENSP00000507496.1:p.Val1165=
ENST00000684010.1:n.3559G=
ENST00000684157.1:n.3564G=
ENST00000684253.1:n.3467G=
ENST00000684288.1:c.*1667G= ENSP00000507143.1:n.*1667G=
ENST00000684313.1:n.2996G=
ENST00000684332.1:n.3637G=
ENST00000684371.1:n.3670G=
ENST00000684404.1:n.3607G=
ENST00000684442.1:n.3564G=
ENST00000684555.1:c.*1707G= ENSP00000507705.1:n.*1707G=
ENST00000684571.1:c.3336G= ENSP00000506935.1:p.Val1112=
ENST00000684593.1:c.*3200G= ENSP00000507005.1:n.*3200G=
ENST00000684711.1:c.*1891G= ENSP00000506841.1:n.*1891G=
ENST00000302539.9:c.3498G= ENSP00000303960.4:p.Val1166=
ENST00000389817.8:c.3495G= MANE Select ENSP00000374467.4:p.Val1165=
ENST00000642271.1:c.3492G= ENSP00000493749.1:p.Val1164=
ENST00000642579.1:c.1579G=
ENST00000642611.1:n.3449G=
ENST00000642902.1:c.3277G=
ENST00000643260.1:c.3495G= ENSP00000494450.1:p.Val1165=
ENST00000643562.1:c.*1471G= ENSP00000496124.1:n.*1471G=
ENST00000643925.1:c.1619G=
ENST00000644447.1:c.1851G= ENSP00000496282.1:p.Val617=
ENST00000644484.1:c.*1750G= ENSP00000493558.1:n.*1750G=
ENST00000644675.1:c.*1667G= ENSP00000494567.1:n.*1667G=
ENST00000644757.1:c.*1780G= ENSP00000495085.1:n.*1780G=
ENST00000644772.1:c.3561G= ENSP00000494321.1:p.Val1187=
ENST00000645004.1:n.634G=
ENST00000645076.1:c.2694G=
ENST00000645417.1:c.661G=
ENST00000645744.1:c.*1759G= ENSP00000494564.1:n.*1759G=
ENST00000645760.1:c.3770G=
ENST00000645884.1:c.*632G= ENSP00000495516.1:n.*632G=
ENST00000646003.1:c.*1451G= ENSP00000495259.1:n.*1451G=
ENST00000646207.1:c.*1962G= ENSP00000495025.1:n.*1962G=
ENST00000646276.1:c.*1768G= ENSP00000496070.1:n.*1768G=
ENST00000646592.1:c.2801G=
ENST00000646902.1:c.3492G= ENSP00000494101.1:p.Val1164=
ENST00000646993.1:c.*1891G= ENSP00000493720.1:n.*1891G=
ENST00000647013.1:c.3501G= ENSP00000496741.1:n.3501G=
ENST00000647015.1:c.3246G= ENSP00000495389.1:p.Val1082=
ENST00000647086.1:c.*3225G= ENSP00000493677.1:n.*3225G=
ENST00000647158.1:c.*1636G= ENSP00000495744.1:n.*1636G=
ENST00000302539.8:c.3498G= ENSP00000303960.4:p.Val1166=
ENST00000389817.7:c.3495G= ENSP00000374467.3:p.Val1165=
ENST00000524561.1:n.627G=
ENST00000527905.5:c.*371G= ENSP00000431653.1:n.*371G=
NM_000352.4:c.3495G= NP_000343.2:p.Val1165=
NM_001287174.1:c.3498G= NP_001274103.1:p.Val1166=
XM_011520331.1:c.3495G= XP_011518633.1:p.Val1165=
XM_011520332.1:c.3498G= XP_011518634.1:p.Val1166=
XM_011520333.1:c.1995G= XP_011518635.1:p.Val665=
XR_930890.1:n.3561G=
XR_930892.1:n.3461G=
XR_930893.1:n.3458G=
NM_001351295.1:c.3561G= NP_001338224.1:p.Val1187=
NM_001351296.1:c.3495G= NP_001338225.1:p.Val1165=
NM_001351297.1:c.3492G= NP_001338226.1:p.Val1164=
NR_147094.1:n.3644G=
XM_017018197.2:c.3564G= XP_016873686.1:p.Val1188=
XM_017018199.1:c.3561G= XP_016873688.1:p.Val1187=
XM_017018201.2:c.3564G= XP_016873690.1:p.Val1188=
XM_017018202.1:c.2061G= XP_016873691.1:p.Val687=
XM_017018204.1:c.1452G= XP_016873693.1:p.Val484=
XM_024448668.1:c.1863G= XP_024304436.1:p.Val621=
XR_001747945.2:n.3636G=
XR_001747946.2:n.3567G=
XR_002957189.1:n.3716G=
NM_000352.6:c.3495G= MANE Select NP_000343.2:p.Val1165=
NM_001287174.2:c.3498G= NP_001274103.1:p.Val1166=
NM_001351295.2:c.3561G= NP_001338224.1:p.Val1187=
NM_001351296.2:c.3495G= NP_001338225.1:p.Val1165=
NM_001351297.2:c.3492G= NP_001338226.1:p.Val1164=
NR_147094.2:n.3644G=
NM_001287174.3:c.3498G= NP_001274103.1:p.Val1166=