Canonical Allele Identifier: CA1955127590
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17404580G= , CM000673.2:g.17404580G= GRCh38
NC_000011.9:g.17426127G= , CM000673.1:g.17426127G= GRCh37
NC_000011.8:g.17382703G= NCBI36
NG_008867.1:g.77323C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.3058C=
ENST00000528374.2:c.68C=
ENST00000529967.6:n.1828C=
ENST00000532220.2:n.1221C=
ENST00000642611.2:n.3558C=
ENST00000645004.2:n.988C=
ENST00000682051.1:n.3505C=
ENST00000682110.1:n.3558C=
ENST00000682140.1:c.3486C= ENSP00000507829.1:p.Phe1162=
ENST00000682185.1:n.4794C=
ENST00000682204.1:c.*1627C= ENSP00000507094.1:n.*1627C=
ENST00000682215.1:n.3555C=
ENST00000682288.1:c.*1920C= ENSP00000507506.1:n.*1920C=
ENST00000682442.1:n.3778C=
ENST00000682528.1:n.3635C=
ENST00000682673.1:n.3502C=
ENST00000682805.1:n.3555C=
ENST00000682965.1:c.3396+914C= ENSP00000508229.1:n.3396+914C=
ENST00000683093.1:n.3657C=
ENST00000683136.1:c.3486C= ENSP00000507768.1:p.Phe1162=
ENST00000683153.1:n.3714C=
ENST00000683365.1:n.3660C=
ENST00000683377.1:n.3558C=
ENST00000683456.1:c.*626C= ENSP00000508318.1:n.*626C=
ENST00000683522.1:n.3558C=
ENST00000683562.1:c.*1658C= ENSP00000508265.1:n.*1658C=
ENST00000683693.1:n.3635C=
ENST00000683725.1:c.3489C= ENSP00000507496.1:p.Phe1163=
ENST00000684010.1:n.3553C=
ENST00000684157.1:n.3558C=
ENST00000684253.1:n.3461C=
ENST00000684288.1:c.*1661C= ENSP00000507143.1:n.*1661C=
ENST00000684313.1:n.2990C=
ENST00000684332.1:n.3631C=
ENST00000684371.1:n.3664C=
ENST00000684404.1:n.3601C=
ENST00000684442.1:n.3558C=
ENST00000684555.1:c.*1701C= ENSP00000507705.1:n.*1701C=
ENST00000684571.1:c.3330C= ENSP00000506935.1:p.Phe1110=
ENST00000684593.1:c.*3194C= ENSP00000507005.1:n.*3194C=
ENST00000684711.1:c.*1885C= ENSP00000506841.1:n.*1885C=
ENST00000302539.9:c.3492C= ENSP00000303960.4:p.Phe1164=
ENST00000389817.8:c.3489C= MANE Select ENSP00000374467.4:p.Phe1163=
ENST00000642271.1:c.3486C= ENSP00000493749.1:p.Phe1162=
ENST00000642579.1:c.1573C=
ENST00000642611.1:n.3443C=
ENST00000642902.1:c.3271C=
ENST00000643260.1:c.3489C= ENSP00000494450.1:p.Phe1163=
ENST00000643562.1:c.*1465C= ENSP00000496124.1:n.*1465C=
ENST00000643925.1:c.1613C=
ENST00000644447.1:c.1845C= ENSP00000496282.1:p.Phe615=
ENST00000644484.1:c.*1744C= ENSP00000493558.1:n.*1744C=
ENST00000644675.1:c.*1661C= ENSP00000494567.1:n.*1661C=
ENST00000644757.1:c.*1774C= ENSP00000495085.1:n.*1774C=
ENST00000644772.1:c.3555C= ENSP00000494321.1:p.Phe1185=
ENST00000645004.1:n.628C=
ENST00000645076.1:c.2688C=
ENST00000645417.1:c.655C=
ENST00000645744.1:c.*1753C= ENSP00000494564.1:n.*1753C=
ENST00000645760.1:c.3764C=
ENST00000645884.1:c.*626C= ENSP00000495516.1:n.*626C=
ENST00000646003.1:c.*1445C= ENSP00000495259.1:n.*1445C=
ENST00000646207.1:c.*1956C= ENSP00000495025.1:n.*1956C=
ENST00000646276.1:c.*1762C= ENSP00000496070.1:n.*1762C=
ENST00000646592.1:c.2795C=
ENST00000646902.1:c.3486C= ENSP00000494101.1:p.Phe1162=
ENST00000646993.1:c.*1885C= ENSP00000493720.1:n.*1885C=
ENST00000647013.1:c.3495C= ENSP00000496741.1:n.3495C=
ENST00000647015.1:c.3240C= ENSP00000495389.1:p.Phe1080=
ENST00000647086.1:c.*3219C= ENSP00000493677.1:n.*3219C=
ENST00000647158.1:c.*1630C= ENSP00000495744.1:n.*1630C=
ENST00000302539.8:c.3492C= ENSP00000303960.4:p.Phe1164=
ENST00000389817.7:c.3489C= ENSP00000374467.3:p.Phe1163=
ENST00000524561.1:n.621C=
ENST00000527905.5:c.*365C= ENSP00000431653.1:n.*365C=
NM_000352.4:c.3489C= NP_000343.2:p.Phe1163=
NM_001287174.1:c.3492C= NP_001274103.1:p.Phe1164=
XM_011520331.1:c.3489C= XP_011518633.1:p.Phe1163=
XM_011520332.1:c.3492C= XP_011518634.1:p.Phe1164=
XM_011520333.1:c.1989C= XP_011518635.1:p.Phe663=
XR_930890.1:n.3555C=
XR_930892.1:n.3455C=
XR_930893.1:n.3452C=
NM_001351295.1:c.3555C= NP_001338224.1:p.Phe1185=
NM_001351296.1:c.3489C= NP_001338225.1:p.Phe1163=
NM_001351297.1:c.3486C= NP_001338226.1:p.Phe1162=
NR_147094.1:n.3638C=
XM_017018197.2:c.3558C= XP_016873686.1:p.Phe1186=
XM_017018199.1:c.3555C= XP_016873688.1:p.Phe1185=
XM_017018201.2:c.3558C= XP_016873690.1:p.Phe1186=
XM_017018202.1:c.2055C= XP_016873691.1:p.Phe685=
XM_017018204.1:c.1446C= XP_016873693.1:p.Phe482=
XM_024448668.1:c.1857C= XP_024304436.1:p.Phe619=
XR_001747945.2:n.3630C=
XR_001747946.2:n.3561C=
XR_002957189.1:n.3710C=
NM_000352.6:c.3489C= MANE Select NP_000343.2:p.Phe1163=
NM_001287174.2:c.3492C= NP_001274103.1:p.Phe1164=
NM_001351295.2:c.3555C= NP_001338224.1:p.Phe1185=
NM_001351296.2:c.3489C= NP_001338225.1:p.Phe1163=
NM_001351297.2:c.3486C= NP_001338226.1:p.Phe1162=
NR_147094.2:n.3638C=
NM_001287174.3:c.3492C= NP_001274103.1:p.Phe1164=