Canonical Allele Identifier: CA1955130262
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17410519G= , CM000673.2:g.17410519G= GRCh38
NC_000011.9:g.17432066G= , CM000673.1:g.17432066G= GRCh37
NC_000011.8:g.17388642G= NCBI36
NG_008867.1:g.71384C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.2360C=
ENST00000529967.6:n.950C=
ENST00000642611.2:n.2760C=
ENST00000682051.1:n.2707C=
ENST00000682110.1:n.2760C=
ENST00000682140.1:c.2688C= ENSP00000507829.1:p.Asp896=
ENST00000682185.1:n.3996C=
ENST00000682204.1:c.*829C= ENSP00000507094.1:n.*829C=
ENST00000682215.1:n.2757C=
ENST00000682288.1:c.*1122C= ENSP00000507506.1:n.*1122C=
ENST00000682442.1:n.2881C=
ENST00000682528.1:n.2757C=
ENST00000682673.1:n.2704C=
ENST00000682805.1:n.2757C=
ENST00000682965.1:c.2688C= ENSP00000508229.1:p.Asp896=
ENST00000683093.1:n.2859C=
ENST00000683136.1:c.2688C= ENSP00000507768.1:p.Asp896=
ENST00000683153.1:n.2916C=
ENST00000683365.1:n.2862C=
ENST00000683377.1:n.2760C=
ENST00000683456.1:c.2691C= ENSP00000508318.1:p.Asp897=
ENST00000683522.1:n.2760C=
ENST00000683562.1:c.*860C= ENSP00000508265.1:n.*860C=
ENST00000683693.1:n.2757C=
ENST00000683725.1:c.2691C= ENSP00000507496.1:p.Asp897=
ENST00000684010.1:n.2675C=
ENST00000684157.1:n.2760C=
ENST00000684253.1:n.2663C=
ENST00000684288.1:c.*863C= ENSP00000507143.1:n.*863C=
ENST00000684313.1:n.2192C=
ENST00000684332.1:n.2833C=
ENST00000684371.1:n.2866C=
ENST00000684404.1:n.2757C=
ENST00000684442.1:n.2760C=
ENST00000684555.1:c.*903C= ENSP00000507705.1:n.*903C=
ENST00000684571.1:c.2532C= ENSP00000506935.1:p.Asp844=
ENST00000684593.1:c.*2396C= ENSP00000507005.1:n.*2396C=
ENST00000684711.1:c.*1087C= ENSP00000506841.1:n.*1087C=
ENST00000302539.9:c.2694C= ENSP00000303960.4:p.Asp898=
ENST00000389817.8:c.2691C= MANE Select ENSP00000374467.4:p.Asp897=
ENST00000642271.1:c.2688C= ENSP00000493749.1:p.Asp896=
ENST00000642579.1:c.775C=
ENST00000642611.1:n.2645C=
ENST00000642902.1:c.2526C=
ENST00000643260.1:c.2691C= ENSP00000494450.1:p.Asp897=
ENST00000643562.1:c.*667C= ENSP00000496124.1:n.*667C=
ENST00000643925.1:c.735C=
ENST00000644447.1:c.1047C= ENSP00000496282.1:p.Asp349=
ENST00000644472.1:c.*1052C= ENSP00000495378.1:n.*1052C=
ENST00000644484.1:c.*900C= ENSP00000493558.1:n.*900C=
ENST00000644542.1:c.*2396C= ENSP00000495532.1:n.*2396C=
ENST00000644675.1:c.*863C= ENSP00000494567.1:n.*863C=
ENST00000644757.1:c.*996C= ENSP00000495085.1:n.*996C=
ENST00000644772.1:c.2757C= ENSP00000494321.1:p.Asp919=
ENST00000645076.1:c.1943C=
ENST00000645744.1:c.*1055C= ENSP00000494564.1:n.*1055C=
ENST00000645760.1:c.2966C=
ENST00000645884.1:c.2691C= ENSP00000495516.1:p.Asp897=
ENST00000646003.1:c.*747C= ENSP00000495259.1:n.*747C=
ENST00000646207.1:c.*1055C= ENSP00000495025.1:n.*1055C=
ENST00000646276.1:c.*964C= ENSP00000496070.1:n.*964C=
ENST00000646592.1:c.1917C=
ENST00000646902.1:c.2688C= ENSP00000494101.1:p.Asp896=
ENST00000646993.1:c.*1087C= ENSP00000493720.1:n.*1087C=
ENST00000647013.1:c.2697C= ENSP00000496741.1:n.2697C=
ENST00000647015.1:c.2442C= ENSP00000495389.1:p.Asp814=
ENST00000647086.1:c.*2421C= ENSP00000493677.1:n.*2421C=
ENST00000647158.1:c.*832C= ENSP00000495744.1:n.*832C=
ENST00000302539.8:c.2694C= ENSP00000303960.4:p.Asp898=
ENST00000389817.7:c.2691C= ENSP00000374467.3:p.Asp897=
ENST00000526921.5:n.375C=
ENST00000527905.5:c.2661C= ENSP00000431653.1:p.Asp887=
ENST00000529967.5:n.360C=
ENST00000530147.5:n.274C=
NM_000352.4:c.2691C= NP_000343.2:p.Asp897=
NM_001287174.1:c.2694C= NP_001274103.1:p.Asp898=
XM_011520331.1:c.2691C= XP_011518633.1:p.Asp897=
XM_011520332.1:c.2694C= XP_011518634.1:p.Asp898=
XM_011520333.1:c.1191C= XP_011518635.1:p.Asp397=
XM_011520334.1:c.2694C= XP_011518636.1:p.Asp898=
XR_930890.1:n.2757C=
XR_930891.1:n.2757C=
XR_930892.1:n.2757C=
XR_930893.1:n.2754C=
NM_001351295.1:c.2757C= NP_001338224.1:p.Asp919=
NM_001351296.1:c.2691C= NP_001338225.1:p.Asp897=
NM_001351297.1:c.2688C= NP_001338226.1:p.Asp896=
NR_147094.1:n.2760C=
XM_017018197.2:c.2760C= XP_016873686.1:p.Asp920=
XM_017018199.1:c.2757C= XP_016873688.1:p.Asp919=
XM_017018201.2:c.2760C= XP_016873690.1:p.Asp920=
XM_017018202.1:c.1257C= XP_016873691.1:p.Asp419=
XM_017018204.1:c.648C= XP_016873693.1:p.Asp216=
XM_024448668.1:c.1059C= XP_024304436.1:p.Asp353=
XR_001747945.2:n.2832C=
XR_001747946.2:n.2763C=
XR_002957189.1:n.2832C=
NM_000352.6:c.2691C= MANE Select NP_000343.2:p.Asp897=
NM_001287174.2:c.2694C= NP_001274103.1:p.Asp898=
NM_001351295.2:c.2757C= NP_001338224.1:p.Asp919=
NM_001351296.2:c.2691C= NP_001338225.1:p.Asp897=
NM_001351297.2:c.2688C= NP_001338226.1:p.Asp896=
NR_147094.2:n.2760C=
NM_001287174.3:c.2694C= NP_001274103.1:p.Asp898=