Canonical Allele Identifier: CA1955127607
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17404615C= , CM000673.2:g.17404615C= GRCh38
NC_000011.9:g.17426162C= , CM000673.1:g.17426162C= GRCh37
NC_000011.8:g.17382738C= NCBI36
NG_008867.1:g.77288G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.3023G=
ENST00000528374.2:c.33G=
ENST00000529967.6:n.1793G=
ENST00000532220.2:n.1186G=
ENST00000642611.2:n.3523G=
ENST00000645004.2:n.953G=
ENST00000682051.1:n.3470G=
ENST00000682110.1:n.3523G=
ENST00000682140.1:c.3451G= ENSP00000507829.1:p.Ala1151=
ENST00000682185.1:n.4759G=
ENST00000682204.1:c.*1592G= ENSP00000507094.1:n.*1592G=
ENST00000682215.1:n.3520G=
ENST00000682288.1:c.*1885G= ENSP00000507506.1:n.*1885G=
ENST00000682442.1:n.3743G=
ENST00000682528.1:n.3600G=
ENST00000682673.1:n.3467G=
ENST00000682805.1:n.3520G=
ENST00000682965.1:c.3396+879G= ENSP00000508229.1:n.3396+879G=
ENST00000683093.1:n.3622G=
ENST00000683136.1:c.3451G= ENSP00000507768.1:p.Ala1151=
ENST00000683153.1:n.3679G=
ENST00000683365.1:n.3625G=
ENST00000683377.1:n.3523G=
ENST00000683456.1:c.*591G= ENSP00000508318.1:n.*591G=
ENST00000683522.1:n.3523G=
ENST00000683562.1:c.*1623G= ENSP00000508265.1:n.*1623G=
ENST00000683693.1:n.3600G=
ENST00000683725.1:c.3454G= ENSP00000507496.1:p.Ala1152=
ENST00000684010.1:n.3518G=
ENST00000684157.1:n.3523G=
ENST00000684253.1:n.3426G=
ENST00000684288.1:c.*1626G= ENSP00000507143.1:n.*1626G=
ENST00000684313.1:n.2955G=
ENST00000684332.1:n.3596G=
ENST00000684371.1:n.3629G=
ENST00000684404.1:n.3566G=
ENST00000684442.1:n.3523G=
ENST00000684555.1:c.*1666G= ENSP00000507705.1:n.*1666G=
ENST00000684571.1:c.3295G= ENSP00000506935.1:p.Ala1099=
ENST00000684593.1:c.*3159G= ENSP00000507005.1:n.*3159G=
ENST00000684711.1:c.*1850G= ENSP00000506841.1:n.*1850G=
ENST00000302539.9:c.3457G= ENSP00000303960.4:p.Ala1153=
ENST00000389817.8:c.3454G= MANE Select ENSP00000374467.4:p.Ala1152=
ENST00000642271.1:c.3451G= ENSP00000493749.1:p.Ala1151=
ENST00000642579.1:c.1538G=
ENST00000642611.1:n.3408G=
ENST00000642902.1:c.3236G=
ENST00000643260.1:c.3454G= ENSP00000494450.1:p.Ala1152=
ENST00000643562.1:c.*1430G= ENSP00000496124.1:n.*1430G=
ENST00000643925.1:c.1578G=
ENST00000644447.1:c.1810G= ENSP00000496282.1:p.Ala604=
ENST00000644484.1:c.*1709G= ENSP00000493558.1:n.*1709G=
ENST00000644675.1:c.*1626G= ENSP00000494567.1:n.*1626G=
ENST00000644757.1:c.*1739G= ENSP00000495085.1:n.*1739G=
ENST00000644772.1:c.3520G= ENSP00000494321.1:p.Ala1174=
ENST00000645004.1:n.593G=
ENST00000645076.1:c.2653G=
ENST00000645417.1:c.620G=
ENST00000645744.1:c.*1718G= ENSP00000494564.1:n.*1718G=
ENST00000645760.1:c.3729G=
ENST00000645884.1:c.*591G= ENSP00000495516.1:n.*591G=
ENST00000646003.1:c.*1410G= ENSP00000495259.1:n.*1410G=
ENST00000646207.1:c.*1921G= ENSP00000495025.1:n.*1921G=
ENST00000646276.1:c.*1727G= ENSP00000496070.1:n.*1727G=
ENST00000646592.1:c.2760G=
ENST00000646902.1:c.3451G= ENSP00000494101.1:p.Ala1151=
ENST00000646993.1:c.*1850G= ENSP00000493720.1:n.*1850G=
ENST00000647013.1:c.3460G= ENSP00000496741.1:n.3460G=
ENST00000647015.1:c.3205G= ENSP00000495389.1:p.Ala1069=
ENST00000647086.1:c.*3184G= ENSP00000493677.1:n.*3184G=
ENST00000647158.1:c.*1595G= ENSP00000495744.1:n.*1595G=
ENST00000302539.8:c.3457G= ENSP00000303960.4:p.Ala1153=
ENST00000389817.7:c.3454G= ENSP00000374467.3:p.Ala1152=
ENST00000524561.1:n.586G=
ENST00000527905.5:c.*330G= ENSP00000431653.1:n.*330G=
NM_000352.4:c.3454G= NP_000343.2:p.Ala1152=
NM_001287174.1:c.3457G= NP_001274103.1:p.Ala1153=
XM_011520331.1:c.3454G= XP_011518633.1:p.Ala1152=
XM_011520332.1:c.3457G= XP_011518634.1:p.Ala1153=
XM_011520333.1:c.1954G= XP_011518635.1:p.Ala652=
XR_930890.1:n.3520G=
XR_930892.1:n.3420G=
XR_930893.1:n.3417G=
NM_001351295.1:c.3520G= NP_001338224.1:p.Ala1174=
NM_001351296.1:c.3454G= NP_001338225.1:p.Ala1152=
NM_001351297.1:c.3451G= NP_001338226.1:p.Ala1151=
NR_147094.1:n.3603G=
XM_017018197.2:c.3523G= XP_016873686.1:p.Ala1175=
XM_017018199.1:c.3520G= XP_016873688.1:p.Ala1174=
XM_017018201.2:c.3523G= XP_016873690.1:p.Ala1175=
XM_017018202.1:c.2020G= XP_016873691.1:p.Ala674=
XM_017018204.1:c.1411G= XP_016873693.1:p.Ala471=
XM_024448668.1:c.1822G= XP_024304436.1:p.Ala608=
XR_001747945.2:n.3595G=
XR_001747946.2:n.3526G=
XR_002957189.1:n.3675G=
NM_000352.6:c.3454G= MANE Select NP_000343.2:p.Ala1152=
NM_001287174.2:c.3457G= NP_001274103.1:p.Ala1153=
NM_001351295.2:c.3520G= NP_001338224.1:p.Ala1174=
NM_001351296.2:c.3454G= NP_001338225.1:p.Ala1152=
NM_001351297.2:c.3451G= NP_001338226.1:p.Ala1151=
NR_147094.2:n.3603G=
NM_001287174.3:c.3457G= NP_001274103.1:p.Ala1153=