Canonical Allele Identifier: CA1955127599
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17404604G= , CM000673.2:g.17404604G= GRCh38
NC_000011.9:g.17426151G= , CM000673.1:g.17426151G= GRCh37
NC_000011.8:g.17382727G= NCBI36
NG_008867.1:g.77299C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.3034C=
ENST00000528374.2:c.44C=
ENST00000529967.6:n.1804C=
ENST00000532220.2:n.1197C=
ENST00000642611.2:n.3534C=
ENST00000645004.2:n.964C=
ENST00000682051.1:n.3481C=
ENST00000682110.1:n.3534C=
ENST00000682140.1:c.3462C= ENSP00000507829.1:p.Val1154=
ENST00000682185.1:n.4770C=
ENST00000682204.1:c.*1603C= ENSP00000507094.1:n.*1603C=
ENST00000682215.1:n.3531C=
ENST00000682288.1:c.*1896C= ENSP00000507506.1:n.*1896C=
ENST00000682442.1:n.3754C=
ENST00000682528.1:n.3611C=
ENST00000682673.1:n.3478C=
ENST00000682805.1:n.3531C=
ENST00000682965.1:c.3396+890C= ENSP00000508229.1:n.3396+890C=
ENST00000683093.1:n.3633C=
ENST00000683136.1:c.3462C= ENSP00000507768.1:p.Val1154=
ENST00000683153.1:n.3690C=
ENST00000683365.1:n.3636C=
ENST00000683377.1:n.3534C=
ENST00000683456.1:c.*602C= ENSP00000508318.1:n.*602C=
ENST00000683522.1:n.3534C=
ENST00000683562.1:c.*1634C= ENSP00000508265.1:n.*1634C=
ENST00000683693.1:n.3611C=
ENST00000683725.1:c.3465C= ENSP00000507496.1:p.Val1155=
ENST00000684010.1:n.3529C=
ENST00000684157.1:n.3534C=
ENST00000684253.1:n.3437C=
ENST00000684288.1:c.*1637C= ENSP00000507143.1:n.*1637C=
ENST00000684313.1:n.2966C=
ENST00000684332.1:n.3607C=
ENST00000684371.1:n.3640C=
ENST00000684404.1:n.3577C=
ENST00000684442.1:n.3534C=
ENST00000684555.1:c.*1677C= ENSP00000507705.1:n.*1677C=
ENST00000684571.1:c.3306C= ENSP00000506935.1:p.Val1102=
ENST00000684593.1:c.*3170C= ENSP00000507005.1:n.*3170C=
ENST00000684711.1:c.*1861C= ENSP00000506841.1:n.*1861C=
ENST00000302539.9:c.3468C= ENSP00000303960.4:p.Val1156=
ENST00000389817.8:c.3465C= MANE Select ENSP00000374467.4:p.Val1155=
ENST00000642271.1:c.3462C= ENSP00000493749.1:p.Val1154=
ENST00000642579.1:c.1549C=
ENST00000642611.1:n.3419C=
ENST00000642902.1:c.3247C=
ENST00000643260.1:c.3465C= ENSP00000494450.1:p.Val1155=
ENST00000643562.1:c.*1441C= ENSP00000496124.1:n.*1441C=
ENST00000643925.1:c.1589C=
ENST00000644447.1:c.1821C= ENSP00000496282.1:p.Val607=
ENST00000644484.1:c.*1720C= ENSP00000493558.1:n.*1720C=
ENST00000644675.1:c.*1637C= ENSP00000494567.1:n.*1637C=
ENST00000644757.1:c.*1750C= ENSP00000495085.1:n.*1750C=
ENST00000644772.1:c.3531C= ENSP00000494321.1:p.Val1177=
ENST00000645004.1:n.604C=
ENST00000645076.1:c.2664C=
ENST00000645417.1:c.631C=
ENST00000645744.1:c.*1729C= ENSP00000494564.1:n.*1729C=
ENST00000645760.1:c.3740C=
ENST00000645884.1:c.*602C= ENSP00000495516.1:n.*602C=
ENST00000646003.1:c.*1421C= ENSP00000495259.1:n.*1421C=
ENST00000646207.1:c.*1932C= ENSP00000495025.1:n.*1932C=
ENST00000646276.1:c.*1738C= ENSP00000496070.1:n.*1738C=
ENST00000646592.1:c.2771C=
ENST00000646902.1:c.3462C= ENSP00000494101.1:p.Val1154=
ENST00000646993.1:c.*1861C= ENSP00000493720.1:n.*1861C=
ENST00000647013.1:c.3471C= ENSP00000496741.1:n.3471C=
ENST00000647015.1:c.3216C= ENSP00000495389.1:p.Val1072=
ENST00000647086.1:c.*3195C= ENSP00000493677.1:n.*3195C=
ENST00000647158.1:c.*1606C= ENSP00000495744.1:n.*1606C=
ENST00000302539.8:c.3468C= ENSP00000303960.4:p.Val1156=
ENST00000389817.7:c.3465C= ENSP00000374467.3:p.Val1155=
ENST00000524561.1:n.597C=
ENST00000527905.5:c.*341C= ENSP00000431653.1:n.*341C=
NM_000352.4:c.3465C= NP_000343.2:p.Val1155=
NM_001287174.1:c.3468C= NP_001274103.1:p.Val1156=
XM_011520331.1:c.3465C= XP_011518633.1:p.Val1155=
XM_011520332.1:c.3468C= XP_011518634.1:p.Val1156=
XM_011520333.1:c.1965C= XP_011518635.1:p.Val655=
XR_930890.1:n.3531C=
XR_930892.1:n.3431C=
XR_930893.1:n.3428C=
NM_001351295.1:c.3531C= NP_001338224.1:p.Val1177=
NM_001351296.1:c.3465C= NP_001338225.1:p.Val1155=
NM_001351297.1:c.3462C= NP_001338226.1:p.Val1154=
NR_147094.1:n.3614C=
XM_017018197.2:c.3534C= XP_016873686.1:p.Val1178=
XM_017018199.1:c.3531C= XP_016873688.1:p.Val1177=
XM_017018201.2:c.3534C= XP_016873690.1:p.Val1178=
XM_017018202.1:c.2031C= XP_016873691.1:p.Val677=
XM_017018204.1:c.1422C= XP_016873693.1:p.Val474=
XM_024448668.1:c.1833C= XP_024304436.1:p.Val611=
XR_001747945.2:n.3606C=
XR_001747946.2:n.3537C=
XR_002957189.1:n.3686C=
NM_000352.6:c.3465C= MANE Select NP_000343.2:p.Val1155=
NM_001287174.2:c.3468C= NP_001274103.1:p.Val1156=
NM_001351295.2:c.3531C= NP_001338224.1:p.Val1177=
NM_001351296.2:c.3465C= NP_001338225.1:p.Val1155=
NM_001351297.2:c.3462C= NP_001338226.1:p.Val1154=
NR_147094.2:n.3614C=
NM_001287174.3:c.3468C= NP_001274103.1:p.Val1156=