Canonical Allele Identifier: CA1955127620
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17404634G= , CM000673.2:g.17404634G= GRCh38
NC_000011.9:g.17426181G= , CM000673.1:g.17426181G= GRCh37
NC_000011.8:g.17382757G= NCBI36
NG_008867.1:g.77269C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.3004C=
ENST00000528374.2:c.14C=
ENST00000529967.6:n.1774C=
ENST00000532220.2:n.1167C=
ENST00000642611.2:n.3504C=
ENST00000645004.2:n.934C=
ENST00000682051.1:n.3451C=
ENST00000682110.1:n.3504C=
ENST00000682140.1:c.3432C= ENSP00000507829.1:p.Ser1144=
ENST00000682185.1:n.4740C=
ENST00000682204.1:c.*1573C= ENSP00000507094.1:n.*1573C=
ENST00000682215.1:n.3501C=
ENST00000682288.1:c.*1866C= ENSP00000507506.1:n.*1866C=
ENST00000682442.1:n.3724C=
ENST00000682528.1:n.3581C=
ENST00000682673.1:n.3448C=
ENST00000682805.1:n.3501C=
ENST00000682965.1:c.3396+860C= ENSP00000508229.1:n.3396+860C=
ENST00000683093.1:n.3603C=
ENST00000683136.1:c.3432C= ENSP00000507768.1:p.Ser1144=
ENST00000683153.1:n.3660C=
ENST00000683365.1:n.3606C=
ENST00000683377.1:n.3504C=
ENST00000683456.1:c.*572C= ENSP00000508318.1:n.*572C=
ENST00000683522.1:n.3504C=
ENST00000683562.1:c.*1604C= ENSP00000508265.1:n.*1604C=
ENST00000683693.1:n.3581C=
ENST00000683725.1:c.3435C= ENSP00000507496.1:p.Ser1145=
ENST00000684010.1:n.3499C=
ENST00000684157.1:n.3504C=
ENST00000684253.1:n.3407C=
ENST00000684288.1:c.*1607C= ENSP00000507143.1:n.*1607C=
ENST00000684313.1:n.2936C=
ENST00000684332.1:n.3577C=
ENST00000684371.1:n.3610C=
ENST00000684404.1:n.3547C=
ENST00000684442.1:n.3504C=
ENST00000684555.1:c.*1647C= ENSP00000507705.1:n.*1647C=
ENST00000684571.1:c.3276C= ENSP00000506935.1:p.Ser1092=
ENST00000684593.1:c.*3140C= ENSP00000507005.1:n.*3140C=
ENST00000684711.1:c.*1831C= ENSP00000506841.1:n.*1831C=
ENST00000302539.9:c.3438C= ENSP00000303960.4:p.Ser1146=
ENST00000389817.8:c.3435C= MANE Select ENSP00000374467.4:p.Ser1145=
ENST00000642271.1:c.3432C= ENSP00000493749.1:p.Ser1144=
ENST00000642579.1:c.1519C=
ENST00000642611.1:n.3389C=
ENST00000642902.1:c.3217C=
ENST00000643260.1:c.3435C= ENSP00000494450.1:p.Ser1145=
ENST00000643562.1:c.*1411C= ENSP00000496124.1:n.*1411C=
ENST00000643925.1:c.1559C=
ENST00000644447.1:c.1791C= ENSP00000496282.1:p.Ser597=
ENST00000644484.1:c.*1690C= ENSP00000493558.1:n.*1690C=
ENST00000644675.1:c.*1607C= ENSP00000494567.1:n.*1607C=
ENST00000644757.1:c.*1720C= ENSP00000495085.1:n.*1720C=
ENST00000644772.1:c.3501C= ENSP00000494321.1:p.Ser1167=
ENST00000645004.1:n.574C=
ENST00000645076.1:c.2634C=
ENST00000645417.1:c.601C=
ENST00000645744.1:c.*1699C= ENSP00000494564.1:n.*1699C=
ENST00000645760.1:c.3710C=
ENST00000645884.1:c.*572C= ENSP00000495516.1:n.*572C=
ENST00000646003.1:c.*1391C= ENSP00000495259.1:n.*1391C=
ENST00000646207.1:c.*1902C= ENSP00000495025.1:n.*1902C=
ENST00000646276.1:c.*1708C= ENSP00000496070.1:n.*1708C=
ENST00000646592.1:c.2741C=
ENST00000646902.1:c.3432C= ENSP00000494101.1:p.Ser1144=
ENST00000646993.1:c.*1831C= ENSP00000493720.1:n.*1831C=
ENST00000647013.1:c.3441C= ENSP00000496741.1:n.3441C=
ENST00000647015.1:c.3186C= ENSP00000495389.1:p.Ser1062=
ENST00000647086.1:c.*3165C= ENSP00000493677.1:n.*3165C=
ENST00000647158.1:c.*1576C= ENSP00000495744.1:n.*1576C=
ENST00000302539.8:c.3438C= ENSP00000303960.4:p.Ser1146=
ENST00000389817.7:c.3435C= ENSP00000374467.3:p.Ser1145=
ENST00000524561.1:n.567C=
ENST00000527905.5:c.*311C= ENSP00000431653.1:n.*311C=
NM_000352.4:c.3435C= NP_000343.2:p.Ser1145=
NM_001287174.1:c.3438C= NP_001274103.1:p.Ser1146=
XM_011520331.1:c.3435C= XP_011518633.1:p.Ser1145=
XM_011520332.1:c.3438C= XP_011518634.1:p.Ser1146=
XM_011520333.1:c.1935C= XP_011518635.1:p.Ser645=
XR_930890.1:n.3501C=
XR_930892.1:n.3401C=
XR_930893.1:n.3398C=
NM_001351295.1:c.3501C= NP_001338224.1:p.Ser1167=
NM_001351296.1:c.3435C= NP_001338225.1:p.Ser1145=
NM_001351297.1:c.3432C= NP_001338226.1:p.Ser1144=
NR_147094.1:n.3584C=
XM_017018197.2:c.3504C= XP_016873686.1:p.Ser1168=
XM_017018199.1:c.3501C= XP_016873688.1:p.Ser1167=
XM_017018201.2:c.3504C= XP_016873690.1:p.Ser1168=
XM_017018202.1:c.2001C= XP_016873691.1:p.Ser667=
XM_017018204.1:c.1392C= XP_016873693.1:p.Ser464=
XM_024448668.1:c.1803C= XP_024304436.1:p.Ser601=
XR_001747945.2:n.3576C=
XR_001747946.2:n.3507C=
XR_002957189.1:n.3656C=
NM_000352.6:c.3435C= MANE Select NP_000343.2:p.Ser1145=
NM_001287174.2:c.3438C= NP_001274103.1:p.Ser1146=
NM_001351295.2:c.3501C= NP_001338224.1:p.Ser1167=
NM_001351296.2:c.3435C= NP_001338225.1:p.Ser1145=
NM_001351297.2:c.3432C= NP_001338226.1:p.Ser1144=
NR_147094.2:n.3584C=
NM_001287174.3:c.3438C= NP_001274103.1:p.Ser1146=