Canonical Allele Identifier: CA1955131328
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17412700C= , CM000673.2:g.17412700C= GRCh38
NC_000011.9:g.17434247C= , CM000673.1:g.17434247C= GRCh37
NC_000011.8:g.17390823C= NCBI36
NG_008867.1:g.69203G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.2191G=
ENST00000529967.6:n.781G=
ENST00000642611.2:n.2591G=
ENST00000682051.1:n.2538G=
ENST00000682110.1:n.2591G=
ENST00000682140.1:c.2519G= ENSP00000507829.1:p.Arg840=
ENST00000682185.1:n.3827G=
ENST00000682204.1:c.*660G= ENSP00000507094.1:n.*660G=
ENST00000682215.1:n.2588G=
ENST00000682288.1:c.*953G= ENSP00000507506.1:n.*953G=
ENST00000682442.1:n.2712G=
ENST00000682528.1:n.2588G=
ENST00000682673.1:n.2535G=
ENST00000682805.1:n.2588G=
ENST00000682965.1:c.2519G= ENSP00000508229.1:p.Arg840=
ENST00000683093.1:n.2690G=
ENST00000683136.1:c.2519G= ENSP00000507768.1:p.Arg840=
ENST00000683153.1:n.2747G=
ENST00000683365.1:n.2693G=
ENST00000683377.1:n.2591G=
ENST00000683456.1:c.2522G= ENSP00000508318.1:p.Arg841=
ENST00000683522.1:n.2591G=
ENST00000683562.1:c.*691G= ENSP00000508265.1:n.*691G=
ENST00000683693.1:n.2588G=
ENST00000683725.1:c.2522G= ENSP00000507496.1:p.Arg841=
ENST00000684010.1:n.2506G=
ENST00000684157.1:n.2591G=
ENST00000684253.1:n.2494G=
ENST00000684288.1:c.*694G= ENSP00000507143.1:n.*694G=
ENST00000684313.1:n.2023G=
ENST00000684332.1:n.2664G=
ENST00000684371.1:n.2697G=
ENST00000684404.1:n.2588G=
ENST00000684442.1:n.2591G=
ENST00000684555.1:c.*734G= ENSP00000507705.1:n.*734G=
ENST00000684571.1:c.2363G= ENSP00000506935.1:p.Arg788=
ENST00000684593.1:c.*2227G= ENSP00000507005.1:n.*2227G=
ENST00000684711.1:c.*918G= ENSP00000506841.1:n.*918G=
ENST00000302539.9:c.2525G= ENSP00000303960.4:p.Arg842=
ENST00000389817.8:c.2522G= MANE Select ENSP00000374467.4:p.Arg841=
ENST00000642271.1:c.2519G= ENSP00000493749.1:p.Arg840=
ENST00000642579.1:c.606G=
ENST00000642611.1:n.2476G=
ENST00000642902.1:c.2357G=
ENST00000643260.1:c.2522G= ENSP00000494450.1:p.Arg841=
ENST00000643562.1:c.*498G= ENSP00000496124.1:n.*498G=
ENST00000643925.1:c.566G=
ENST00000644447.1:c.878G= ENSP00000496282.1:p.Arg293=
ENST00000644472.1:c.*883G= ENSP00000495378.1:n.*883G=
ENST00000644484.1:c.*731G= ENSP00000493558.1:n.*731G=
ENST00000644542.1:c.*2227G= ENSP00000495532.1:n.*2227G=
ENST00000644675.1:c.*694G= ENSP00000494567.1:n.*694G=
ENST00000644757.1:c.*827G= ENSP00000495085.1:n.*827G=
ENST00000644772.1:c.2588G= ENSP00000494321.1:p.Arg863=
ENST00000645076.1:c.1774G=
ENST00000645744.1:c.*886G= ENSP00000494564.1:n.*886G=
ENST00000645760.1:c.2797G=
ENST00000645884.1:c.2522G= ENSP00000495516.1:p.Arg841=
ENST00000646003.1:c.*578G= ENSP00000495259.1:n.*578G=
ENST00000646207.1:c.*886G= ENSP00000495025.1:n.*886G=
ENST00000646276.1:c.*795G= ENSP00000496070.1:n.*795G=
ENST00000646592.1:c.1748G=
ENST00000646902.1:c.2519G= ENSP00000494101.1:p.Arg840=
ENST00000646993.1:c.*918G= ENSP00000493720.1:n.*918G=
ENST00000647013.1:c.2528G= ENSP00000496741.1:n.2528G=
ENST00000647015.1:c.2273G= ENSP00000495389.1:p.Arg758=
ENST00000647086.1:c.*2252G= ENSP00000493677.1:n.*2252G=
ENST00000647158.1:c.*663G= ENSP00000495744.1:n.*663G=
ENST00000302539.8:c.2525G= ENSP00000303960.4:p.Arg842=
ENST00000389817.7:c.2522G= ENSP00000374467.3:p.Arg841=
ENST00000526921.5:n.206G=
ENST00000527905.5:c.2492G= ENSP00000431653.1:p.Arg831=
ENST00000529967.5:n.191G=
ENST00000530147.5:n.105G=
ENST00000531911.1:n.636G=
NM_000352.4:c.2522G= NP_000343.2:p.Arg841=
NM_001287174.1:c.2525G= NP_001274103.1:p.Arg842=
XM_011520331.1:c.2522G= XP_011518633.1:p.Arg841=
XM_011520332.1:c.2525G= XP_011518634.1:p.Arg842=
XM_011520333.1:c.1022G= XP_011518635.1:p.Arg341=
XM_011520334.1:c.2525G= XP_011518636.1:p.Arg842=
XR_930890.1:n.2588G=
XR_930891.1:n.2588G=
XR_930892.1:n.2588G=
XR_930893.1:n.2585G=
NM_001351295.1:c.2588G= NP_001338224.1:p.Arg863=
NM_001351296.1:c.2522G= NP_001338225.1:p.Arg841=
NM_001351297.1:c.2519G= NP_001338226.1:p.Arg840=
NR_147094.1:n.2591G=
XM_017018197.2:c.2591G= XP_016873686.1:p.Arg864=
XM_017018199.1:c.2588G= XP_016873688.1:p.Arg863=
XM_017018201.2:c.2591G= XP_016873690.1:p.Arg864=
XM_017018202.1:c.1088G= XP_016873691.1:p.Arg363=
XM_017018204.1:c.479G= XP_016873693.1:p.Arg160=
XM_024448668.1:c.890G= XP_024304436.1:p.Arg297=
XR_001747945.2:n.2663G=
XR_001747946.2:n.2594G=
XR_002957189.1:n.2663G=
NM_000352.6:c.2522G= MANE Select NP_000343.2:p.Arg841=
NM_001287174.2:c.2525G= NP_001274103.1:p.Arg842=
NM_001351295.2:c.2588G= NP_001338224.1:p.Arg863=
NM_001351296.2:c.2522G= NP_001338225.1:p.Arg841=
NM_001351297.2:c.2519G= NP_001338226.1:p.Arg840=
NR_147094.2:n.2591G=
NM_001287174.3:c.2525G= NP_001274103.1:p.Arg842=