Canonical Allele Identifier: CA1955127589
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17404577G= , CM000673.2:g.17404577G= GRCh38
NC_000011.9:g.17426124G= , CM000673.1:g.17426124G= GRCh37
NC_000011.8:g.17382700G= NCBI36
NG_008867.1:g.77326C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.3061C=
ENST00000528374.2:c.71C=
ENST00000529967.6:n.1831C=
ENST00000532220.2:n.1224C=
ENST00000642611.2:n.3561C=
ENST00000645004.2:n.991C=
ENST00000682051.1:n.3508C=
ENST00000682110.1:n.3561C=
ENST00000682140.1:c.3489C= ENSP00000507829.1:p.Leu1163=
ENST00000682185.1:n.4797C=
ENST00000682204.1:c.*1630C= ENSP00000507094.1:n.*1630C=
ENST00000682215.1:n.3558C=
ENST00000682288.1:c.*1923C= ENSP00000507506.1:n.*1923C=
ENST00000682442.1:n.3781C=
ENST00000682528.1:n.3638C=
ENST00000682673.1:n.3505C=
ENST00000682805.1:n.3558C=
ENST00000682965.1:c.3396+917C= ENSP00000508229.1:n.3396+917C=
ENST00000683093.1:n.3660C=
ENST00000683136.1:c.3489C= ENSP00000507768.1:p.Leu1163=
ENST00000683153.1:n.3717C=
ENST00000683365.1:n.3663C=
ENST00000683377.1:n.3561C=
ENST00000683456.1:c.*629C= ENSP00000508318.1:n.*629C=
ENST00000683522.1:n.3561C=
ENST00000683562.1:c.*1661C= ENSP00000508265.1:n.*1661C=
ENST00000683693.1:n.3638C=
ENST00000683725.1:c.3492C= ENSP00000507496.1:p.Leu1164=
ENST00000684010.1:n.3556C=
ENST00000684157.1:n.3561C=
ENST00000684253.1:n.3464C=
ENST00000684288.1:c.*1664C= ENSP00000507143.1:n.*1664C=
ENST00000684313.1:n.2993C=
ENST00000684332.1:n.3634C=
ENST00000684371.1:n.3667C=
ENST00000684404.1:n.3604C=
ENST00000684442.1:n.3561C=
ENST00000684555.1:c.*1704C= ENSP00000507705.1:n.*1704C=
ENST00000684571.1:c.3333C= ENSP00000506935.1:p.Leu1111=
ENST00000684593.1:c.*3197C= ENSP00000507005.1:n.*3197C=
ENST00000684711.1:c.*1888C= ENSP00000506841.1:n.*1888C=
ENST00000302539.9:c.3495C= ENSP00000303960.4:p.Leu1165=
ENST00000389817.8:c.3492C= MANE Select ENSP00000374467.4:p.Leu1164=
ENST00000642271.1:c.3489C= ENSP00000493749.1:p.Leu1163=
ENST00000642579.1:c.1576C=
ENST00000642611.1:n.3446C=
ENST00000642902.1:c.3274C=
ENST00000643260.1:c.3492C= ENSP00000494450.1:p.Leu1164=
ENST00000643562.1:c.*1468C= ENSP00000496124.1:n.*1468C=
ENST00000643925.1:c.1616C=
ENST00000644447.1:c.1848C= ENSP00000496282.1:p.Leu616=
ENST00000644484.1:c.*1747C= ENSP00000493558.1:n.*1747C=
ENST00000644675.1:c.*1664C= ENSP00000494567.1:n.*1664C=
ENST00000644757.1:c.*1777C= ENSP00000495085.1:n.*1777C=
ENST00000644772.1:c.3558C= ENSP00000494321.1:p.Leu1186=
ENST00000645004.1:n.631C=
ENST00000645076.1:c.2691C=
ENST00000645417.1:c.658C=
ENST00000645744.1:c.*1756C= ENSP00000494564.1:n.*1756C=
ENST00000645760.1:c.3767C=
ENST00000645884.1:c.*629C= ENSP00000495516.1:n.*629C=
ENST00000646003.1:c.*1448C= ENSP00000495259.1:n.*1448C=
ENST00000646207.1:c.*1959C= ENSP00000495025.1:n.*1959C=
ENST00000646276.1:c.*1765C= ENSP00000496070.1:n.*1765C=
ENST00000646592.1:c.2798C=
ENST00000646902.1:c.3489C= ENSP00000494101.1:p.Leu1163=
ENST00000646993.1:c.*1888C= ENSP00000493720.1:n.*1888C=
ENST00000647013.1:c.3498C= ENSP00000496741.1:n.3498C=
ENST00000647015.1:c.3243C= ENSP00000495389.1:p.Leu1081=
ENST00000647086.1:c.*3222C= ENSP00000493677.1:n.*3222C=
ENST00000647158.1:c.*1633C= ENSP00000495744.1:n.*1633C=
ENST00000302539.8:c.3495C= ENSP00000303960.4:p.Leu1165=
ENST00000389817.7:c.3492C= ENSP00000374467.3:p.Leu1164=
ENST00000524561.1:n.624C=
ENST00000527905.5:c.*368C= ENSP00000431653.1:n.*368C=
NM_000352.4:c.3492C= NP_000343.2:p.Leu1164=
NM_001287174.1:c.3495C= NP_001274103.1:p.Leu1165=
XM_011520331.1:c.3492C= XP_011518633.1:p.Leu1164=
XM_011520332.1:c.3495C= XP_011518634.1:p.Leu1165=
XM_011520333.1:c.1992C= XP_011518635.1:p.Leu664=
XR_930890.1:n.3558C=
XR_930892.1:n.3458C=
XR_930893.1:n.3455C=
NM_001351295.1:c.3558C= NP_001338224.1:p.Leu1186=
NM_001351296.1:c.3492C= NP_001338225.1:p.Leu1164=
NM_001351297.1:c.3489C= NP_001338226.1:p.Leu1163=
NR_147094.1:n.3641C=
XM_017018197.2:c.3561C= XP_016873686.1:p.Leu1187=
XM_017018199.1:c.3558C= XP_016873688.1:p.Leu1186=
XM_017018201.2:c.3561C= XP_016873690.1:p.Leu1187=
XM_017018202.1:c.2058C= XP_016873691.1:p.Leu686=
XM_017018204.1:c.1449C= XP_016873693.1:p.Leu483=
XM_024448668.1:c.1860C= XP_024304436.1:p.Leu620=
XR_001747945.2:n.3633C=
XR_001747946.2:n.3564C=
XR_002957189.1:n.3713C=
NM_000352.6:c.3492C= MANE Select NP_000343.2:p.Leu1164=
NM_001287174.2:c.3495C= NP_001274103.1:p.Leu1165=
NM_001351295.2:c.3558C= NP_001338224.1:p.Leu1186=
NM_001351296.2:c.3492C= NP_001338225.1:p.Leu1164=
NM_001351297.2:c.3489C= NP_001338226.1:p.Leu1163=
NR_147094.2:n.3641C=
NM_001287174.3:c.3495C= NP_001274103.1:p.Leu1165=