Canonical Allele Identifier: CA1955127602
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17404608G= , CM000673.2:g.17404608G= GRCh38
NC_000011.9:g.17426155G= , CM000673.1:g.17426155G= GRCh37
NC_000011.8:g.17382731G= NCBI36
NG_008867.1:g.77295C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.3030C=
ENST00000528374.2:c.40C=
ENST00000529967.6:n.1800C=
ENST00000532220.2:n.1193C=
ENST00000642611.2:n.3530C=
ENST00000645004.2:n.960C=
ENST00000682051.1:n.3477C=
ENST00000682110.1:n.3530C=
ENST00000682140.1:c.3458C= ENSP00000507829.1:p.Ala1153=
ENST00000682185.1:n.4766C=
ENST00000682204.1:c.*1599C= ENSP00000507094.1:n.*1599C=
ENST00000682215.1:n.3527C=
ENST00000682288.1:c.*1892C= ENSP00000507506.1:n.*1892C=
ENST00000682442.1:n.3750C=
ENST00000682528.1:n.3607C=
ENST00000682673.1:n.3474C=
ENST00000682805.1:n.3527C=
ENST00000682965.1:c.3396+886C= ENSP00000508229.1:n.3396+886C=
ENST00000683093.1:n.3629C=
ENST00000683136.1:c.3458C= ENSP00000507768.1:p.Ala1153=
ENST00000683153.1:n.3686C=
ENST00000683365.1:n.3632C=
ENST00000683377.1:n.3530C=
ENST00000683456.1:c.*598C= ENSP00000508318.1:n.*598C=
ENST00000683522.1:n.3530C=
ENST00000683562.1:c.*1630C= ENSP00000508265.1:n.*1630C=
ENST00000683693.1:n.3607C=
ENST00000683725.1:c.3461C= ENSP00000507496.1:p.Ala1154=
ENST00000684010.1:n.3525C=
ENST00000684157.1:n.3530C=
ENST00000684253.1:n.3433C=
ENST00000684288.1:c.*1633C= ENSP00000507143.1:n.*1633C=
ENST00000684313.1:n.2962C=
ENST00000684332.1:n.3603C=
ENST00000684371.1:n.3636C=
ENST00000684404.1:n.3573C=
ENST00000684442.1:n.3530C=
ENST00000684555.1:c.*1673C= ENSP00000507705.1:n.*1673C=
ENST00000684571.1:c.3302C= ENSP00000506935.1:p.Ala1101=
ENST00000684593.1:c.*3166C= ENSP00000507005.1:n.*3166C=
ENST00000684711.1:c.*1857C= ENSP00000506841.1:n.*1857C=
ENST00000302539.9:c.3464C= ENSP00000303960.4:p.Ala1155=
ENST00000389817.8:c.3461C= MANE Select ENSP00000374467.4:p.Ala1154=
ENST00000642271.1:c.3458C= ENSP00000493749.1:p.Ala1153=
ENST00000642579.1:c.1545C=
ENST00000642611.1:n.3415C=
ENST00000642902.1:c.3243C=
ENST00000643260.1:c.3461C= ENSP00000494450.1:p.Ala1154=
ENST00000643562.1:c.*1437C= ENSP00000496124.1:n.*1437C=
ENST00000643925.1:c.1585C=
ENST00000644447.1:c.1817C= ENSP00000496282.1:p.Ala606=
ENST00000644484.1:c.*1716C= ENSP00000493558.1:n.*1716C=
ENST00000644675.1:c.*1633C= ENSP00000494567.1:n.*1633C=
ENST00000644757.1:c.*1746C= ENSP00000495085.1:n.*1746C=
ENST00000644772.1:c.3527C= ENSP00000494321.1:p.Ala1176=
ENST00000645004.1:n.600C=
ENST00000645076.1:c.2660C=
ENST00000645417.1:c.627C=
ENST00000645744.1:c.*1725C= ENSP00000494564.1:n.*1725C=
ENST00000645760.1:c.3736C=
ENST00000645884.1:c.*598C= ENSP00000495516.1:n.*598C=
ENST00000646003.1:c.*1417C= ENSP00000495259.1:n.*1417C=
ENST00000646207.1:c.*1928C= ENSP00000495025.1:n.*1928C=
ENST00000646276.1:c.*1734C= ENSP00000496070.1:n.*1734C=
ENST00000646592.1:c.2767C=
ENST00000646902.1:c.3458C= ENSP00000494101.1:p.Ala1153=
ENST00000646993.1:c.*1857C= ENSP00000493720.1:n.*1857C=
ENST00000647013.1:c.3467C= ENSP00000496741.1:n.3467C=
ENST00000647015.1:c.3212C= ENSP00000495389.1:p.Ala1071=
ENST00000647086.1:c.*3191C= ENSP00000493677.1:n.*3191C=
ENST00000647158.1:c.*1602C= ENSP00000495744.1:n.*1602C=
ENST00000302539.8:c.3464C= ENSP00000303960.4:p.Ala1155=
ENST00000389817.7:c.3461C= ENSP00000374467.3:p.Ala1154=
ENST00000524561.1:n.593C=
ENST00000527905.5:c.*337C= ENSP00000431653.1:n.*337C=
NM_000352.4:c.3461C= NP_000343.2:p.Ala1154=
NM_001287174.1:c.3464C= NP_001274103.1:p.Ala1155=
XM_011520331.1:c.3461C= XP_011518633.1:p.Ala1154=
XM_011520332.1:c.3464C= XP_011518634.1:p.Ala1155=
XM_011520333.1:c.1961C= XP_011518635.1:p.Ala654=
XR_930890.1:n.3527C=
XR_930892.1:n.3427C=
XR_930893.1:n.3424C=
NM_001351295.1:c.3527C= NP_001338224.1:p.Ala1176=
NM_001351296.1:c.3461C= NP_001338225.1:p.Ala1154=
NM_001351297.1:c.3458C= NP_001338226.1:p.Ala1153=
NR_147094.1:n.3610C=
XM_017018197.2:c.3530C= XP_016873686.1:p.Ala1177=
XM_017018199.1:c.3527C= XP_016873688.1:p.Ala1176=
XM_017018201.2:c.3530C= XP_016873690.1:p.Ala1177=
XM_017018202.1:c.2027C= XP_016873691.1:p.Ala676=
XM_017018204.1:c.1418C= XP_016873693.1:p.Ala473=
XM_024448668.1:c.1829C= XP_024304436.1:p.Ala610=
XR_001747945.2:n.3602C=
XR_001747946.2:n.3533C=
XR_002957189.1:n.3682C=
NM_000352.6:c.3461C= MANE Select NP_000343.2:p.Ala1154=
NM_001287174.2:c.3464C= NP_001274103.1:p.Ala1155=
NM_001351295.2:c.3527C= NP_001338224.1:p.Ala1176=
NM_001351296.2:c.3461C= NP_001338225.1:p.Ala1154=
NM_001351297.2:c.3458C= NP_001338226.1:p.Ala1153=
NR_147094.2:n.3610C=
NM_001287174.3:c.3464C= NP_001274103.1:p.Ala1155=