Canonical Allele Identifier: CA1955127611
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17404622A= , CM000673.2:g.17404622A= GRCh38
NC_000011.9:g.17426169A= , CM000673.1:g.17426169A= GRCh37
NC_000011.8:g.17382745A= NCBI36
NG_008867.1:g.77281T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.3016T=
ENST00000528374.2:c.26T=
ENST00000529967.6:n.1786T=
ENST00000532220.2:n.1179T=
ENST00000642611.2:n.3516T=
ENST00000645004.2:n.946T=
ENST00000682051.1:n.3463T=
ENST00000682110.1:n.3516T=
ENST00000682140.1:c.3444T= ENSP00000507829.1:p.Cys1148=
ENST00000682185.1:n.4752T=
ENST00000682204.1:c.*1585T= ENSP00000507094.1:n.*1585T=
ENST00000682215.1:n.3513T=
ENST00000682288.1:c.*1878T= ENSP00000507506.1:n.*1878T=
ENST00000682442.1:n.3736T=
ENST00000682528.1:n.3593T=
ENST00000682673.1:n.3460T=
ENST00000682805.1:n.3513T=
ENST00000682965.1:c.3396+872T= ENSP00000508229.1:n.3396+872T=
ENST00000683093.1:n.3615T=
ENST00000683136.1:c.3444T= ENSP00000507768.1:p.Cys1148=
ENST00000683153.1:n.3672T=
ENST00000683365.1:n.3618T=
ENST00000683377.1:n.3516T=
ENST00000683456.1:c.*584T= ENSP00000508318.1:n.*584T=
ENST00000683522.1:n.3516T=
ENST00000683562.1:c.*1616T= ENSP00000508265.1:n.*1616T=
ENST00000683693.1:n.3593T=
ENST00000683725.1:c.3447T= ENSP00000507496.1:p.Cys1149=
ENST00000684010.1:n.3511T=
ENST00000684157.1:n.3516T=
ENST00000684253.1:n.3419T=
ENST00000684288.1:c.*1619T= ENSP00000507143.1:n.*1619T=
ENST00000684313.1:n.2948T=
ENST00000684332.1:n.3589T=
ENST00000684371.1:n.3622T=
ENST00000684404.1:n.3559T=
ENST00000684442.1:n.3516T=
ENST00000684555.1:c.*1659T= ENSP00000507705.1:n.*1659T=
ENST00000684571.1:c.3288T= ENSP00000506935.1:p.Cys1096=
ENST00000684593.1:c.*3152T= ENSP00000507005.1:n.*3152T=
ENST00000684711.1:c.*1843T= ENSP00000506841.1:n.*1843T=
ENST00000302539.9:c.3450T= ENSP00000303960.4:p.Cys1150=
ENST00000389817.8:c.3447T= MANE Select ENSP00000374467.4:p.Cys1149=
ENST00000642271.1:c.3444T= ENSP00000493749.1:p.Cys1148=
ENST00000642579.1:c.1531T=
ENST00000642611.1:n.3401T=
ENST00000642902.1:c.3229T=
ENST00000643260.1:c.3447T= ENSP00000494450.1:p.Cys1149=
ENST00000643562.1:c.*1423T= ENSP00000496124.1:n.*1423T=
ENST00000643925.1:c.1571T=
ENST00000644447.1:c.1803T= ENSP00000496282.1:p.Cys601=
ENST00000644484.1:c.*1702T= ENSP00000493558.1:n.*1702T=
ENST00000644675.1:c.*1619T= ENSP00000494567.1:n.*1619T=
ENST00000644757.1:c.*1732T= ENSP00000495085.1:n.*1732T=
ENST00000644772.1:c.3513T= ENSP00000494321.1:p.Cys1171=
ENST00000645004.1:n.586T=
ENST00000645076.1:c.2646T=
ENST00000645417.1:c.613T=
ENST00000645744.1:c.*1711T= ENSP00000494564.1:n.*1711T=
ENST00000645760.1:c.3722T=
ENST00000645884.1:c.*584T= ENSP00000495516.1:n.*584T=
ENST00000646003.1:c.*1403T= ENSP00000495259.1:n.*1403T=
ENST00000646207.1:c.*1914T= ENSP00000495025.1:n.*1914T=
ENST00000646276.1:c.*1720T= ENSP00000496070.1:n.*1720T=
ENST00000646592.1:c.2753T=
ENST00000646902.1:c.3444T= ENSP00000494101.1:p.Cys1148=
ENST00000646993.1:c.*1843T= ENSP00000493720.1:n.*1843T=
ENST00000647013.1:c.3453T= ENSP00000496741.1:n.3453T=
ENST00000647015.1:c.3198T= ENSP00000495389.1:p.Cys1066=
ENST00000647086.1:c.*3177T= ENSP00000493677.1:n.*3177T=
ENST00000647158.1:c.*1588T= ENSP00000495744.1:n.*1588T=
ENST00000302539.8:c.3450T= ENSP00000303960.4:p.Cys1150=
ENST00000389817.7:c.3447T= ENSP00000374467.3:p.Cys1149=
ENST00000524561.1:n.579T=
ENST00000527905.5:c.*323T= ENSP00000431653.1:n.*323T=
NM_000352.4:c.3447T= NP_000343.2:p.Cys1149=
NM_001287174.1:c.3450T= NP_001274103.1:p.Cys1150=
XM_011520331.1:c.3447T= XP_011518633.1:p.Cys1149=
XM_011520332.1:c.3450T= XP_011518634.1:p.Cys1150=
XM_011520333.1:c.1947T= XP_011518635.1:p.Cys649=
XR_930890.1:n.3513T=
XR_930892.1:n.3413T=
XR_930893.1:n.3410T=
NM_001351295.1:c.3513T= NP_001338224.1:p.Cys1171=
NM_001351296.1:c.3447T= NP_001338225.1:p.Cys1149=
NM_001351297.1:c.3444T= NP_001338226.1:p.Cys1148=
NR_147094.1:n.3596T=
XM_017018197.2:c.3516T= XP_016873686.1:p.Cys1172=
XM_017018199.1:c.3513T= XP_016873688.1:p.Cys1171=
XM_017018201.2:c.3516T= XP_016873690.1:p.Cys1172=
XM_017018202.1:c.2013T= XP_016873691.1:p.Cys671=
XM_017018204.1:c.1404T= XP_016873693.1:p.Cys468=
XM_024448668.1:c.1815T= XP_024304436.1:p.Cys605=
XR_001747945.2:n.3588T=
XR_001747946.2:n.3519T=
XR_002957189.1:n.3668T=
NM_000352.6:c.3447T= MANE Select NP_000343.2:p.Cys1149=
NM_001287174.2:c.3450T= NP_001274103.1:p.Cys1150=
NM_001351295.2:c.3513T= NP_001338224.1:p.Cys1171=
NM_001351296.2:c.3447T= NP_001338225.1:p.Cys1149=
NM_001351297.2:c.3444T= NP_001338226.1:p.Cys1148=
NR_147094.2:n.3596T=
NM_001287174.3:c.3450T= NP_001274103.1:p.Cys1150=