Canonical Allele Identifier: CA1955128495
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17406659G= , CM000673.2:g.17406659G= GRCh38
NC_000011.9:g.17428206G= , CM000673.1:g.17428206G= GRCh37
NC_000011.8:g.17384782G= NCBI36
NG_008867.1:g.75244C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.2861C=
ENST00000529967.6:n.1631C=
ENST00000532220.2:n.1024C=
ENST00000642611.2:n.3361C=
ENST00000645004.2:n.791C=
ENST00000682051.1:n.3308C=
ENST00000682110.1:n.3361C=
ENST00000682140.1:c.3289C= ENSP00000507829.1:p.Arg1097=
ENST00000682185.1:n.4597C=
ENST00000682204.1:c.*1430C= ENSP00000507094.1:n.*1430C=
ENST00000682215.1:n.3358C=
ENST00000682288.1:c.*1723C= ENSP00000507506.1:n.*1723C=
ENST00000682442.1:n.3581C=
ENST00000682528.1:n.3438C=
ENST00000682673.1:n.3305C=
ENST00000682805.1:n.3358C=
ENST00000682965.1:c.3289C= ENSP00000508229.1:p.Arg1097=
ENST00000683093.1:n.3460C=
ENST00000683136.1:c.3289C= ENSP00000507768.1:p.Arg1097=
ENST00000683153.1:n.3517C=
ENST00000683365.1:n.3463C=
ENST00000683377.1:n.3361C=
ENST00000683456.1:c.*429C= ENSP00000508318.1:n.*429C=
ENST00000683522.1:n.3361C=
ENST00000683562.1:c.*1461C= ENSP00000508265.1:n.*1461C=
ENST00000683693.1:n.3438C=
ENST00000683725.1:c.3292C= ENSP00000507496.1:p.Arg1098=
ENST00000684010.1:n.3356C=
ENST00000684157.1:n.3361C=
ENST00000684253.1:n.3264C=
ENST00000684288.1:c.*1464C= ENSP00000507143.1:n.*1464C=
ENST00000684313.1:n.2793C=
ENST00000684332.1:n.3434C=
ENST00000684371.1:n.3467C=
ENST00000684404.1:n.3404C=
ENST00000684442.1:n.3361C=
ENST00000684555.1:c.*1504C= ENSP00000507705.1:n.*1504C=
ENST00000684571.1:c.3133C= ENSP00000506935.1:p.Arg1045=
ENST00000684593.1:c.*2997C= ENSP00000507005.1:n.*2997C=
ENST00000684711.1:c.*1688C= ENSP00000506841.1:n.*1688C=
ENST00000302539.9:c.3295C= ENSP00000303960.4:p.Arg1099=
ENST00000389817.8:c.3292C= MANE Select ENSP00000374467.4:p.Arg1098=
ENST00000642271.1:c.3289C= ENSP00000493749.1:p.Arg1097=
ENST00000642579.1:c.1376C=
ENST00000642611.1:n.3246C=
ENST00000642902.1:c.3074C=
ENST00000643260.1:c.3292C= ENSP00000494450.1:p.Arg1098=
ENST00000643562.1:c.*1268C= ENSP00000496124.1:n.*1268C=
ENST00000643925.1:c.1416C=
ENST00000644447.1:c.1648C= ENSP00000496282.1:p.Arg550=
ENST00000644484.1:c.*1547C= ENSP00000493558.1:n.*1547C=
ENST00000644542.1:c.*3096C= ENSP00000495532.1:n.*3096C=
ENST00000644675.1:c.*1464C= ENSP00000494567.1:n.*1464C=
ENST00000644757.1:c.*1577C= ENSP00000495085.1:n.*1577C=
ENST00000644772.1:c.3358C= ENSP00000494321.1:p.Arg1120=
ENST00000645004.1:n.431C=
ENST00000645076.1:c.2491C=
ENST00000645417.1:c.458C=
ENST00000645744.1:c.*1556C= ENSP00000494564.1:n.*1556C=
ENST00000645760.1:c.3567C=
ENST00000645884.1:c.*429C= ENSP00000495516.1:n.*429C=
ENST00000646003.1:c.*1248C= ENSP00000495259.1:n.*1248C=
ENST00000646207.1:c.*1759C= ENSP00000495025.1:n.*1759C=
ENST00000646276.1:c.*1565C= ENSP00000496070.1:n.*1565C=
ENST00000646592.1:c.2598C=
ENST00000646902.1:c.3289C= ENSP00000494101.1:p.Arg1097=
ENST00000646993.1:c.*1688C= ENSP00000493720.1:n.*1688C=
ENST00000647013.1:c.3298C= ENSP00000496741.1:n.3298C=
ENST00000647015.1:c.3043C= ENSP00000495389.1:p.Arg1015=
ENST00000647086.1:c.*3022C= ENSP00000493677.1:n.*3022C=
ENST00000647158.1:c.*1433C= ENSP00000495744.1:n.*1433C=
ENST00000302539.8:c.3295C= ENSP00000303960.4:p.Arg1099=
ENST00000389817.7:c.3292C= ENSP00000374467.3:p.Arg1098=
ENST00000524561.1:n.424C=
ENST00000527905.5:c.*168C= ENSP00000431653.1:n.*168C=
NM_000352.4:c.3292C= NP_000343.2:p.Arg1098=
NM_001287174.1:c.3295C= NP_001274103.1:p.Arg1099=
XM_011520331.1:c.3292C= XP_011518633.1:p.Arg1098=
XM_011520332.1:c.3295C= XP_011518634.1:p.Arg1099=
XM_011520333.1:c.1792C= XP_011518635.1:p.Arg598=
XR_930890.1:n.3358C=
XR_930891.1:n.3358C=
XR_930892.1:n.3258C=
XR_930893.1:n.3255C=
NM_001351295.1:c.3358C= NP_001338224.1:p.Arg1120=
NM_001351296.1:c.3292C= NP_001338225.1:p.Arg1098=
NM_001351297.1:c.3289C= NP_001338226.1:p.Arg1097=
NR_147094.1:n.3441C=
XM_017018197.2:c.3361C= XP_016873686.1:p.Arg1121=
XM_017018199.1:c.3358C= XP_016873688.1:p.Arg1120=
XM_017018201.2:c.3361C= XP_016873690.1:p.Arg1121=
XM_017018202.1:c.1858C= XP_016873691.1:p.Arg620=
XM_017018204.1:c.1249C= XP_016873693.1:p.Arg417=
XM_024448668.1:c.1660C= XP_024304436.1:p.Arg554=
XR_001747945.2:n.3433C=
XR_001747946.2:n.3364C=
XR_002957189.1:n.3513C=
NM_000352.6:c.3292C= MANE Select NP_000343.2:p.Arg1098=
NM_001287174.2:c.3295C= NP_001274103.1:p.Arg1099=
NM_001351295.2:c.3358C= NP_001338224.1:p.Arg1120=
NM_001351296.2:c.3292C= NP_001338225.1:p.Arg1098=
NM_001351297.2:c.3289C= NP_001338226.1:p.Arg1097=
NR_147094.2:n.3441C=
NM_001287174.3:c.3295C= NP_001274103.1:p.Arg1099=