Canonical Allele Identifier: CA1955128494
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17406658C= , CM000673.2:g.17406658C= GRCh38
NC_000011.9:g.17428205C= , CM000673.1:g.17428205C= GRCh37
NC_000011.8:g.17384781C= NCBI36
NG_008867.1:g.75245G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.2862G=
ENST00000529967.6:n.1632G=
ENST00000532220.2:n.1025G=
ENST00000642611.2:n.3362G=
ENST00000645004.2:n.792G=
ENST00000682051.1:n.3309G=
ENST00000682110.1:n.3362G=
ENST00000682140.1:c.3290G= ENSP00000507829.1:p.Arg1097=
ENST00000682185.1:n.4598G=
ENST00000682204.1:c.*1431G= ENSP00000507094.1:n.*1431G=
ENST00000682215.1:n.3359G=
ENST00000682288.1:c.*1724G= ENSP00000507506.1:n.*1724G=
ENST00000682442.1:n.3582G=
ENST00000682528.1:n.3439G=
ENST00000682673.1:n.3306G=
ENST00000682805.1:n.3359G=
ENST00000682965.1:c.3290G= ENSP00000508229.1:p.Arg1097=
ENST00000683093.1:n.3461G=
ENST00000683136.1:c.3290G= ENSP00000507768.1:p.Arg1097=
ENST00000683153.1:n.3518G=
ENST00000683365.1:n.3464G=
ENST00000683377.1:n.3362G=
ENST00000683456.1:c.*430G= ENSP00000508318.1:n.*430G=
ENST00000683522.1:n.3362G=
ENST00000683562.1:c.*1462G= ENSP00000508265.1:n.*1462G=
ENST00000683693.1:n.3439G=
ENST00000683725.1:c.3293G= ENSP00000507496.1:p.Arg1098=
ENST00000684010.1:n.3357G=
ENST00000684157.1:n.3362G=
ENST00000684253.1:n.3265G=
ENST00000684288.1:c.*1465G= ENSP00000507143.1:n.*1465G=
ENST00000684313.1:n.2794G=
ENST00000684332.1:n.3435G=
ENST00000684371.1:n.3468G=
ENST00000684404.1:n.3405G=
ENST00000684442.1:n.3362G=
ENST00000684555.1:c.*1505G= ENSP00000507705.1:n.*1505G=
ENST00000684571.1:c.3134G= ENSP00000506935.1:p.Arg1045=
ENST00000684593.1:c.*2998G= ENSP00000507005.1:n.*2998G=
ENST00000684711.1:c.*1689G= ENSP00000506841.1:n.*1689G=
ENST00000302539.9:c.3296G= ENSP00000303960.4:p.Arg1099=
ENST00000389817.8:c.3293G= MANE Select ENSP00000374467.4:p.Arg1098=
ENST00000642271.1:c.3290G= ENSP00000493749.1:p.Arg1097=
ENST00000642579.1:c.1377G=
ENST00000642611.1:n.3247G=
ENST00000642902.1:c.3075G=
ENST00000643260.1:c.3293G= ENSP00000494450.1:p.Arg1098=
ENST00000643562.1:c.*1269G= ENSP00000496124.1:n.*1269G=
ENST00000643925.1:c.1417G=
ENST00000644447.1:c.1649G= ENSP00000496282.1:p.Arg550=
ENST00000644484.1:c.*1548G= ENSP00000493558.1:n.*1548G=
ENST00000644542.1:c.*3097G= ENSP00000495532.1:n.*3097G=
ENST00000644675.1:c.*1465G= ENSP00000494567.1:n.*1465G=
ENST00000644757.1:c.*1578G= ENSP00000495085.1:n.*1578G=
ENST00000644772.1:c.3359G= ENSP00000494321.1:p.Arg1120=
ENST00000645004.1:n.432G=
ENST00000645076.1:c.2492G=
ENST00000645417.1:c.459G=
ENST00000645744.1:c.*1557G= ENSP00000494564.1:n.*1557G=
ENST00000645760.1:c.3568G=
ENST00000645884.1:c.*430G= ENSP00000495516.1:n.*430G=
ENST00000646003.1:c.*1249G= ENSP00000495259.1:n.*1249G=
ENST00000646207.1:c.*1760G= ENSP00000495025.1:n.*1760G=
ENST00000646276.1:c.*1566G= ENSP00000496070.1:n.*1566G=
ENST00000646592.1:c.2599G=
ENST00000646902.1:c.3290G= ENSP00000494101.1:p.Arg1097=
ENST00000646993.1:c.*1689G= ENSP00000493720.1:n.*1689G=
ENST00000647013.1:c.3299G= ENSP00000496741.1:n.3299G=
ENST00000647015.1:c.3044G= ENSP00000495389.1:p.Arg1015=
ENST00000647086.1:c.*3023G= ENSP00000493677.1:n.*3023G=
ENST00000647158.1:c.*1434G= ENSP00000495744.1:n.*1434G=
ENST00000302539.8:c.3296G= ENSP00000303960.4:p.Arg1099=
ENST00000389817.7:c.3293G= ENSP00000374467.3:p.Arg1098=
ENST00000524561.1:n.425G=
ENST00000527905.5:c.*169G= ENSP00000431653.1:n.*169G=
NM_000352.4:c.3293G= NP_000343.2:p.Arg1098=
NM_001287174.1:c.3296G= NP_001274103.1:p.Arg1099=
XM_011520331.1:c.3293G= XP_011518633.1:p.Arg1098=
XM_011520332.1:c.3296G= XP_011518634.1:p.Arg1099=
XM_011520333.1:c.1793G= XP_011518635.1:p.Arg598=
XR_930890.1:n.3359G=
XR_930891.1:n.3359G=
XR_930892.1:n.3259G=
XR_930893.1:n.3256G=
NM_001351295.1:c.3359G= NP_001338224.1:p.Arg1120=
NM_001351296.1:c.3293G= NP_001338225.1:p.Arg1098=
NM_001351297.1:c.3290G= NP_001338226.1:p.Arg1097=
NR_147094.1:n.3442G=
XM_017018197.2:c.3362G= XP_016873686.1:p.Arg1121=
XM_017018199.1:c.3359G= XP_016873688.1:p.Arg1120=
XM_017018201.2:c.3362G= XP_016873690.1:p.Arg1121=
XM_017018202.1:c.1859G= XP_016873691.1:p.Arg620=
XM_017018204.1:c.1250G= XP_016873693.1:p.Arg417=
XM_024448668.1:c.1661G= XP_024304436.1:p.Arg554=
XR_001747945.2:n.3434G=
XR_001747946.2:n.3365G=
XR_002957189.1:n.3514G=
NM_000352.6:c.3293G= MANE Select NP_000343.2:p.Arg1098=
NM_001287174.2:c.3296G= NP_001274103.1:p.Arg1099=
NM_001351295.2:c.3359G= NP_001338224.1:p.Arg1120=
NM_001351296.2:c.3293G= NP_001338225.1:p.Arg1098=
NM_001351297.2:c.3290G= NP_001338226.1:p.Arg1097=
NR_147094.2:n.3442G=
NM_001287174.3:c.3296G= NP_001274103.1:p.Arg1099=