Canonical Allele Identifier: CA1955127591
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17404583C= , CM000673.2:g.17404583C= GRCh38
NC_000011.9:g.17426130C= , CM000673.1:g.17426130C= GRCh37
NC_000011.8:g.17382706C= NCBI36
NG_008867.1:g.77320G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.3055G=
ENST00000528374.2:c.65G=
ENST00000529967.6:n.1825G=
ENST00000532220.2:n.1218G=
ENST00000642611.2:n.3555G=
ENST00000645004.2:n.985G=
ENST00000682051.1:n.3502G=
ENST00000682110.1:n.3555G=
ENST00000682140.1:c.3483G= ENSP00000507829.1:p.Val1161=
ENST00000682185.1:n.4791G=
ENST00000682204.1:c.*1624G= ENSP00000507094.1:n.*1624G=
ENST00000682215.1:n.3552G=
ENST00000682288.1:c.*1917G= ENSP00000507506.1:n.*1917G=
ENST00000682442.1:n.3775G=
ENST00000682528.1:n.3632G=
ENST00000682673.1:n.3499G=
ENST00000682805.1:n.3552G=
ENST00000682965.1:c.3396+911G= ENSP00000508229.1:n.3396+911G=
ENST00000683093.1:n.3654G=
ENST00000683136.1:c.3483G= ENSP00000507768.1:p.Val1161=
ENST00000683153.1:n.3711G=
ENST00000683365.1:n.3657G=
ENST00000683377.1:n.3555G=
ENST00000683456.1:c.*623G= ENSP00000508318.1:n.*623G=
ENST00000683522.1:n.3555G=
ENST00000683562.1:c.*1655G= ENSP00000508265.1:n.*1655G=
ENST00000683693.1:n.3632G=
ENST00000683725.1:c.3486G= ENSP00000507496.1:p.Val1162=
ENST00000684010.1:n.3550G=
ENST00000684157.1:n.3555G=
ENST00000684253.1:n.3458G=
ENST00000684288.1:c.*1658G= ENSP00000507143.1:n.*1658G=
ENST00000684313.1:n.2987G=
ENST00000684332.1:n.3628G=
ENST00000684371.1:n.3661G=
ENST00000684404.1:n.3598G=
ENST00000684442.1:n.3555G=
ENST00000684555.1:c.*1698G= ENSP00000507705.1:n.*1698G=
ENST00000684571.1:c.3327G= ENSP00000506935.1:p.Val1109=
ENST00000684593.1:c.*3191G= ENSP00000507005.1:n.*3191G=
ENST00000684711.1:c.*1882G= ENSP00000506841.1:n.*1882G=
ENST00000302539.9:c.3489G= ENSP00000303960.4:p.Val1163=
ENST00000389817.8:c.3486G= MANE Select ENSP00000374467.4:p.Val1162=
ENST00000642271.1:c.3483G= ENSP00000493749.1:p.Val1161=
ENST00000642579.1:c.1570G=
ENST00000642611.1:n.3440G=
ENST00000642902.1:c.3268G=
ENST00000643260.1:c.3486G= ENSP00000494450.1:p.Val1162=
ENST00000643562.1:c.*1462G= ENSP00000496124.1:n.*1462G=
ENST00000643925.1:c.1610G=
ENST00000644447.1:c.1842G= ENSP00000496282.1:p.Val614=
ENST00000644484.1:c.*1741G= ENSP00000493558.1:n.*1741G=
ENST00000644675.1:c.*1658G= ENSP00000494567.1:n.*1658G=
ENST00000644757.1:c.*1771G= ENSP00000495085.1:n.*1771G=
ENST00000644772.1:c.3552G= ENSP00000494321.1:p.Val1184=
ENST00000645004.1:n.625G=
ENST00000645076.1:c.2685G=
ENST00000645417.1:c.652G=
ENST00000645744.1:c.*1750G= ENSP00000494564.1:n.*1750G=
ENST00000645760.1:c.3761G=
ENST00000645884.1:c.*623G= ENSP00000495516.1:n.*623G=
ENST00000646003.1:c.*1442G= ENSP00000495259.1:n.*1442G=
ENST00000646207.1:c.*1953G= ENSP00000495025.1:n.*1953G=
ENST00000646276.1:c.*1759G= ENSP00000496070.1:n.*1759G=
ENST00000646592.1:c.2792G=
ENST00000646902.1:c.3483G= ENSP00000494101.1:p.Val1161=
ENST00000646993.1:c.*1882G= ENSP00000493720.1:n.*1882G=
ENST00000647013.1:c.3492G= ENSP00000496741.1:n.3492G=
ENST00000647015.1:c.3237G= ENSP00000495389.1:p.Val1079=
ENST00000647086.1:c.*3216G= ENSP00000493677.1:n.*3216G=
ENST00000647158.1:c.*1627G= ENSP00000495744.1:n.*1627G=
ENST00000302539.8:c.3489G= ENSP00000303960.4:p.Val1163=
ENST00000389817.7:c.3486G= ENSP00000374467.3:p.Val1162=
ENST00000524561.1:n.618G=
ENST00000527905.5:c.*362G= ENSP00000431653.1:n.*362G=
NM_000352.4:c.3486G= NP_000343.2:p.Val1162=
NM_001287174.1:c.3489G= NP_001274103.1:p.Val1163=
XM_011520331.1:c.3486G= XP_011518633.1:p.Val1162=
XM_011520332.1:c.3489G= XP_011518634.1:p.Val1163=
XM_011520333.1:c.1986G= XP_011518635.1:p.Val662=
XR_930890.1:n.3552G=
XR_930892.1:n.3452G=
XR_930893.1:n.3449G=
NM_001351295.1:c.3552G= NP_001338224.1:p.Val1184=
NM_001351296.1:c.3486G= NP_001338225.1:p.Val1162=
NM_001351297.1:c.3483G= NP_001338226.1:p.Val1161=
NR_147094.1:n.3635G=
XM_017018197.2:c.3555G= XP_016873686.1:p.Val1185=
XM_017018199.1:c.3552G= XP_016873688.1:p.Val1184=
XM_017018201.2:c.3555G= XP_016873690.1:p.Val1185=
XM_017018202.1:c.2052G= XP_016873691.1:p.Val684=
XM_017018204.1:c.1443G= XP_016873693.1:p.Val481=
XM_024448668.1:c.1854G= XP_024304436.1:p.Val618=
XR_001747945.2:n.3627G=
XR_001747946.2:n.3558G=
XR_002957189.1:n.3707G=
NM_000352.6:c.3486G= MANE Select NP_000343.2:p.Val1162=
NM_001287174.2:c.3489G= NP_001274103.1:p.Val1163=
NM_001351295.2:c.3552G= NP_001338224.1:p.Val1184=
NM_001351296.2:c.3486G= NP_001338225.1:p.Val1162=
NM_001351297.2:c.3483G= NP_001338226.1:p.Val1161=
NR_147094.2:n.3635G=
NM_001287174.3:c.3489G= NP_001274103.1:p.Val1163=