Canonical Allele Identifier: CA1955128489
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17406645G= , CM000673.2:g.17406645G= GRCh38
NC_000011.9:g.17428192G= , CM000673.1:g.17428192G= GRCh37
NC_000011.8:g.17384768G= NCBI36
NG_008867.1:g.75258C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.2875C=
ENST00000529967.6:n.1645C=
ENST00000532220.2:n.1038C=
ENST00000642611.2:n.3375C=
ENST00000645004.2:n.805C=
ENST00000682051.1:n.3322C=
ENST00000682110.1:n.3375C=
ENST00000682140.1:c.3303C= ENSP00000507829.1:p.Asn1101=
ENST00000682185.1:n.4611C=
ENST00000682204.1:c.*1444C= ENSP00000507094.1:n.*1444C=
ENST00000682215.1:n.3372C=
ENST00000682288.1:c.*1737C= ENSP00000507506.1:n.*1737C=
ENST00000682442.1:n.3595C=
ENST00000682528.1:n.3452C=
ENST00000682673.1:n.3319C=
ENST00000682805.1:n.3372C=
ENST00000682965.1:c.3303C= ENSP00000508229.1:p.Asn1101=
ENST00000683093.1:n.3474C=
ENST00000683136.1:c.3303C= ENSP00000507768.1:p.Asn1101=
ENST00000683153.1:n.3531C=
ENST00000683365.1:n.3477C=
ENST00000683377.1:n.3375C=
ENST00000683456.1:c.*443C= ENSP00000508318.1:n.*443C=
ENST00000683522.1:n.3375C=
ENST00000683562.1:c.*1475C= ENSP00000508265.1:n.*1475C=
ENST00000683693.1:n.3452C=
ENST00000683725.1:c.3306C= ENSP00000507496.1:p.Asn1102=
ENST00000684010.1:n.3370C=
ENST00000684157.1:n.3375C=
ENST00000684253.1:n.3278C=
ENST00000684288.1:c.*1478C= ENSP00000507143.1:n.*1478C=
ENST00000684313.1:n.2807C=
ENST00000684332.1:n.3448C=
ENST00000684371.1:n.3481C=
ENST00000684404.1:n.3418C=
ENST00000684442.1:n.3375C=
ENST00000684555.1:c.*1518C= ENSP00000507705.1:n.*1518C=
ENST00000684571.1:c.3147C= ENSP00000506935.1:p.Asn1049=
ENST00000684593.1:c.*3011C= ENSP00000507005.1:n.*3011C=
ENST00000684711.1:c.*1702C= ENSP00000506841.1:n.*1702C=
ENST00000302539.9:c.3309C= ENSP00000303960.4:p.Asn1103=
ENST00000389817.8:c.3306C= MANE Select ENSP00000374467.4:p.Asn1102=
ENST00000642271.1:c.3303C= ENSP00000493749.1:p.Asn1101=
ENST00000642579.1:c.1390C=
ENST00000642611.1:n.3260C=
ENST00000642902.1:c.3088C=
ENST00000643260.1:c.3306C= ENSP00000494450.1:p.Asn1102=
ENST00000643562.1:c.*1282C= ENSP00000496124.1:n.*1282C=
ENST00000643925.1:c.1430C=
ENST00000644447.1:c.1662C= ENSP00000496282.1:p.Asn554=
ENST00000644484.1:c.*1561C= ENSP00000493558.1:n.*1561C=
ENST00000644542.1:c.*3110C= ENSP00000495532.1:n.*3110C=
ENST00000644675.1:c.*1478C= ENSP00000494567.1:n.*1478C=
ENST00000644757.1:c.*1591C= ENSP00000495085.1:n.*1591C=
ENST00000644772.1:c.3372C= ENSP00000494321.1:p.Asn1124=
ENST00000645004.1:n.445C=
ENST00000645076.1:c.2505C=
ENST00000645417.1:c.472C=
ENST00000645744.1:c.*1570C= ENSP00000494564.1:n.*1570C=
ENST00000645760.1:c.3581C=
ENST00000645884.1:c.*443C= ENSP00000495516.1:n.*443C=
ENST00000646003.1:c.*1262C= ENSP00000495259.1:n.*1262C=
ENST00000646207.1:c.*1773C= ENSP00000495025.1:n.*1773C=
ENST00000646276.1:c.*1579C= ENSP00000496070.1:n.*1579C=
ENST00000646592.1:c.2612C=
ENST00000646902.1:c.3303C= ENSP00000494101.1:p.Asn1101=
ENST00000646993.1:c.*1702C= ENSP00000493720.1:n.*1702C=
ENST00000647013.1:c.3312C= ENSP00000496741.1:n.3312C=
ENST00000647015.1:c.3057C= ENSP00000495389.1:p.Asn1019=
ENST00000647086.1:c.*3036C= ENSP00000493677.1:n.*3036C=
ENST00000647158.1:c.*1447C= ENSP00000495744.1:n.*1447C=
ENST00000302539.8:c.3309C= ENSP00000303960.4:p.Asn1103=
ENST00000389817.7:c.3306C= ENSP00000374467.3:p.Asn1102=
ENST00000524561.1:n.438C=
ENST00000527905.5:c.*182C= ENSP00000431653.1:n.*182C=
NM_000352.4:c.3306C= NP_000343.2:p.Asn1102=
NM_001287174.1:c.3309C= NP_001274103.1:p.Asn1103=
XM_011520331.1:c.3306C= XP_011518633.1:p.Asn1102=
XM_011520332.1:c.3309C= XP_011518634.1:p.Asn1103=
XM_011520333.1:c.1806C= XP_011518635.1:p.Asn602=
XR_930890.1:n.3372C=
XR_930891.1:n.3372C=
XR_930892.1:n.3272C=
XR_930893.1:n.3269C=
NM_001351295.1:c.3372C= NP_001338224.1:p.Asn1124=
NM_001351296.1:c.3306C= NP_001338225.1:p.Asn1102=
NM_001351297.1:c.3303C= NP_001338226.1:p.Asn1101=
NR_147094.1:n.3455C=
XM_017018197.2:c.3375C= XP_016873686.1:p.Asn1125=
XM_017018199.1:c.3372C= XP_016873688.1:p.Asn1124=
XM_017018201.2:c.3375C= XP_016873690.1:p.Asn1125=
XM_017018202.1:c.1872C= XP_016873691.1:p.Asn624=
XM_017018204.1:c.1263C= XP_016873693.1:p.Asn421=
XM_024448668.1:c.1674C= XP_024304436.1:p.Asn558=
XR_001747945.2:n.3447C=
XR_001747946.2:n.3378C=
XR_002957189.1:n.3527C=
NM_000352.6:c.3306C= MANE Select NP_000343.2:p.Asn1102=
NM_001287174.2:c.3309C= NP_001274103.1:p.Asn1103=
NM_001351295.2:c.3372C= NP_001338224.1:p.Asn1124=
NM_001351296.2:c.3306C= NP_001338225.1:p.Asn1102=
NM_001351297.2:c.3303C= NP_001338226.1:p.Asn1101=
NR_147094.2:n.3455C=
NM_001287174.3:c.3309C= NP_001274103.1:p.Asn1103=