Canonical Allele Identifier: CA1955131332
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17412709C= , CM000673.2:g.17412709C= GRCh38
NC_000011.9:g.17434256C= , CM000673.1:g.17434256C= GRCh37
NC_000011.8:g.17390832C= NCBI36
NG_008867.1:g.69194G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.2182G=
ENST00000529967.6:n.772G=
ENST00000642611.2:n.2582G=
ENST00000682051.1:n.2529G=
ENST00000682110.1:n.2582G=
ENST00000682140.1:c.2510G= ENSP00000507829.1:p.Ser837=
ENST00000682185.1:n.3818G=
ENST00000682204.1:c.*651G= ENSP00000507094.1:n.*651G=
ENST00000682215.1:n.2579G=
ENST00000682288.1:c.*944G= ENSP00000507506.1:n.*944G=
ENST00000682442.1:n.2703G=
ENST00000682528.1:n.2579G=
ENST00000682673.1:n.2526G=
ENST00000682805.1:n.2579G=
ENST00000682965.1:c.2510G= ENSP00000508229.1:p.Ser837=
ENST00000683093.1:n.2681G=
ENST00000683136.1:c.2510G= ENSP00000507768.1:p.Ser837=
ENST00000683153.1:n.2738G=
ENST00000683365.1:n.2684G=
ENST00000683377.1:n.2582G=
ENST00000683456.1:c.2513G= ENSP00000508318.1:p.Ser838=
ENST00000683522.1:n.2582G=
ENST00000683562.1:c.*682G= ENSP00000508265.1:n.*682G=
ENST00000683693.1:n.2579G=
ENST00000683725.1:c.2513G= ENSP00000507496.1:p.Ser838=
ENST00000684010.1:n.2497G=
ENST00000684157.1:n.2582G=
ENST00000684253.1:n.2485G=
ENST00000684288.1:c.*685G= ENSP00000507143.1:n.*685G=
ENST00000684313.1:n.2014G=
ENST00000684332.1:n.2655G=
ENST00000684371.1:n.2688G=
ENST00000684404.1:n.2579G=
ENST00000684442.1:n.2582G=
ENST00000684555.1:c.*725G= ENSP00000507705.1:n.*725G=
ENST00000684571.1:c.2354G= ENSP00000506935.1:p.Ser785=
ENST00000684593.1:c.*2218G= ENSP00000507005.1:n.*2218G=
ENST00000684711.1:c.*909G= ENSP00000506841.1:n.*909G=
ENST00000302539.9:c.2516G= ENSP00000303960.4:p.Ser839=
ENST00000389817.8:c.2513G= MANE Select ENSP00000374467.4:p.Ser838=
ENST00000642271.1:c.2510G= ENSP00000493749.1:p.Ser837=
ENST00000642579.1:c.597G=
ENST00000642611.1:n.2467G=
ENST00000642902.1:c.2348G=
ENST00000643260.1:c.2513G= ENSP00000494450.1:p.Ser838=
ENST00000643562.1:c.*489G= ENSP00000496124.1:n.*489G=
ENST00000643925.1:c.557G=
ENST00000644447.1:c.869G= ENSP00000496282.1:p.Ser290=
ENST00000644472.1:c.*874G= ENSP00000495378.1:n.*874G=
ENST00000644484.1:c.*722G= ENSP00000493558.1:n.*722G=
ENST00000644542.1:c.*2218G= ENSP00000495532.1:n.*2218G=
ENST00000644675.1:c.*685G= ENSP00000494567.1:n.*685G=
ENST00000644757.1:c.*818G= ENSP00000495085.1:n.*818G=
ENST00000644772.1:c.2579G= ENSP00000494321.1:p.Ser860=
ENST00000645076.1:c.1765G=
ENST00000645744.1:c.*877G= ENSP00000494564.1:n.*877G=
ENST00000645760.1:c.2788G=
ENST00000645884.1:c.2513G= ENSP00000495516.1:p.Ser838=
ENST00000646003.1:c.*569G= ENSP00000495259.1:n.*569G=
ENST00000646207.1:c.*877G= ENSP00000495025.1:n.*877G=
ENST00000646276.1:c.*786G= ENSP00000496070.1:n.*786G=
ENST00000646592.1:c.1739G=
ENST00000646902.1:c.2510G= ENSP00000494101.1:p.Ser837=
ENST00000646993.1:c.*909G= ENSP00000493720.1:n.*909G=
ENST00000647013.1:c.2519G= ENSP00000496741.1:n.2519G=
ENST00000647015.1:c.2264G= ENSP00000495389.1:p.Ser755=
ENST00000647086.1:c.*2243G= ENSP00000493677.1:n.*2243G=
ENST00000647158.1:c.*654G= ENSP00000495744.1:n.*654G=
ENST00000302539.8:c.2516G= ENSP00000303960.4:p.Ser839=
ENST00000389817.7:c.2513G= ENSP00000374467.3:p.Ser838=
ENST00000526921.5:n.197G=
ENST00000527905.5:c.2483G= ENSP00000431653.1:p.Ser828=
ENST00000529967.5:n.182G=
ENST00000530147.5:n.96G=
ENST00000531911.1:n.627G=
NM_000352.4:c.2513G= NP_000343.2:p.Ser838=
NM_001287174.1:c.2516G= NP_001274103.1:p.Ser839=
XM_011520331.1:c.2513G= XP_011518633.1:p.Ser838=
XM_011520332.1:c.2516G= XP_011518634.1:p.Ser839=
XM_011520333.1:c.1013G= XP_011518635.1:p.Ser338=
XM_011520334.1:c.2516G= XP_011518636.1:p.Ser839=
XR_930890.1:n.2579G=
XR_930891.1:n.2579G=
XR_930892.1:n.2579G=
XR_930893.1:n.2576G=
NM_001351295.1:c.2579G= NP_001338224.1:p.Ser860=
NM_001351296.1:c.2513G= NP_001338225.1:p.Ser838=
NM_001351297.1:c.2510G= NP_001338226.1:p.Ser837=
NR_147094.1:n.2582G=
XM_017018197.2:c.2582G= XP_016873686.1:p.Ser861=
XM_017018199.1:c.2579G= XP_016873688.1:p.Ser860=
XM_017018201.2:c.2582G= XP_016873690.1:p.Ser861=
XM_017018202.1:c.1079G= XP_016873691.1:p.Ser360=
XM_017018204.1:c.470G= XP_016873693.1:p.Ser157=
XM_024448668.1:c.881G= XP_024304436.1:p.Ser294=
XR_001747945.2:n.2654G=
XR_001747946.2:n.2585G=
XR_002957189.1:n.2654G=
NM_000352.6:c.2513G= MANE Select NP_000343.2:p.Ser838=
NM_001287174.2:c.2516G= NP_001274103.1:p.Ser839=
NM_001351295.2:c.2579G= NP_001338224.1:p.Ser860=
NM_001351296.2:c.2513G= NP_001338225.1:p.Ser838=
NM_001351297.2:c.2510G= NP_001338226.1:p.Ser837=
NR_147094.2:n.2582G=
NM_001287174.3:c.2516G= NP_001274103.1:p.Ser839=