Canonical Allele Identifier: CA1955131345
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17412745C= , CM000673.2:g.17412745C= GRCh38
NC_000011.9:g.17434292C= , CM000673.1:g.17434292C= GRCh37
NC_000011.8:g.17390868C= NCBI36
NG_008867.1:g.69158G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.2146G=
ENST00000529967.6:n.736G=
ENST00000642611.2:n.2546G=
ENST00000682051.1:n.2493G=
ENST00000682110.1:n.2546G=
ENST00000682140.1:c.2474G= ENSP00000507829.1:p.Gly825=
ENST00000682185.1:n.3782G=
ENST00000682204.1:c.*615G= ENSP00000507094.1:n.*615G=
ENST00000682215.1:n.2543G=
ENST00000682288.1:c.*908G= ENSP00000507506.1:n.*908G=
ENST00000682442.1:n.2667G=
ENST00000682528.1:n.2543G=
ENST00000682673.1:n.2490G=
ENST00000682805.1:n.2543G=
ENST00000682965.1:c.2474G= ENSP00000508229.1:p.Gly825=
ENST00000683093.1:n.2645G=
ENST00000683136.1:c.2474G= ENSP00000507768.1:p.Gly825=
ENST00000683153.1:n.2702G=
ENST00000683365.1:n.2648G=
ENST00000683377.1:n.2546G=
ENST00000683456.1:c.2477G= ENSP00000508318.1:p.Gly826=
ENST00000683522.1:n.2546G=
ENST00000683562.1:c.*646G= ENSP00000508265.1:n.*646G=
ENST00000683693.1:n.2543G=
ENST00000683725.1:c.2477G= ENSP00000507496.1:p.Gly826=
ENST00000684010.1:n.2461G=
ENST00000684157.1:n.2546G=
ENST00000684253.1:n.2449G=
ENST00000684288.1:c.*649G= ENSP00000507143.1:n.*649G=
ENST00000684313.1:n.1978G=
ENST00000684332.1:n.2619G=
ENST00000684371.1:n.2652G=
ENST00000684404.1:n.2543G=
ENST00000684442.1:n.2546G=
ENST00000684555.1:c.*689G= ENSP00000507705.1:n.*689G=
ENST00000684571.1:c.2318G= ENSP00000506935.1:p.Gly773=
ENST00000684593.1:c.*2182G= ENSP00000507005.1:n.*2182G=
ENST00000684711.1:c.*873G= ENSP00000506841.1:n.*873G=
ENST00000302539.9:c.2480G= ENSP00000303960.4:p.Gly827=
ENST00000389817.8:c.2477G= MANE Select ENSP00000374467.4:p.Gly826=
ENST00000642271.1:c.2474G= ENSP00000493749.1:p.Gly825=
ENST00000642579.1:c.561G=
ENST00000642611.1:n.2431G=
ENST00000642902.1:c.2312G=
ENST00000643260.1:c.2477G= ENSP00000494450.1:p.Gly826=
ENST00000643562.1:c.*453G= ENSP00000496124.1:n.*453G=
ENST00000643925.1:c.521G=
ENST00000644447.1:c.833G= ENSP00000496282.1:p.Gly278=
ENST00000644472.1:c.*838G= ENSP00000495378.1:n.*838G=
ENST00000644484.1:c.*686G= ENSP00000493558.1:n.*686G=
ENST00000644542.1:c.*2182G= ENSP00000495532.1:n.*2182G=
ENST00000644675.1:c.*649G= ENSP00000494567.1:n.*649G=
ENST00000644757.1:c.*782G= ENSP00000495085.1:n.*782G=
ENST00000644772.1:c.2543G= ENSP00000494321.1:p.Gly848=
ENST00000645076.1:c.1729G=
ENST00000645744.1:c.*841G= ENSP00000494564.1:n.*841G=
ENST00000645760.1:c.2752G=
ENST00000645884.1:c.2477G= ENSP00000495516.1:p.Gly826=
ENST00000646003.1:c.*533G= ENSP00000495259.1:n.*533G=
ENST00000646207.1:c.*841G= ENSP00000495025.1:n.*841G=
ENST00000646276.1:c.*750G= ENSP00000496070.1:n.*750G=
ENST00000646592.1:c.1703G=
ENST00000646902.1:c.2474G= ENSP00000494101.1:p.Gly825=
ENST00000646993.1:c.*873G= ENSP00000493720.1:n.*873G=
ENST00000647013.1:c.2483G= ENSP00000496741.1:n.2483G=
ENST00000647015.1:c.2228G= ENSP00000495389.1:p.Gly743=
ENST00000647086.1:c.*2207G= ENSP00000493677.1:n.*2207G=
ENST00000647158.1:c.*618G= ENSP00000495744.1:n.*618G=
ENST00000302539.8:c.2480G= ENSP00000303960.4:p.Gly827=
ENST00000389817.7:c.2477G= ENSP00000374467.3:p.Gly826=
ENST00000526921.5:n.161G=
ENST00000527905.5:c.2447G= ENSP00000431653.1:p.Gly816=
ENST00000529967.5:n.146G=
ENST00000530147.5:n.60G=
ENST00000531911.1:n.591G=
NM_000352.4:c.2477G= NP_000343.2:p.Gly826=
NM_001287174.1:c.2480G= NP_001274103.1:p.Gly827=
XM_011520331.1:c.2477G= XP_011518633.1:p.Gly826=
XM_011520332.1:c.2480G= XP_011518634.1:p.Gly827=
XM_011520333.1:c.977G= XP_011518635.1:p.Gly326=
XM_011520334.1:c.2480G= XP_011518636.1:p.Gly827=
XR_930890.1:n.2543G=
XR_930891.1:n.2543G=
XR_930892.1:n.2543G=
XR_930893.1:n.2540G=
NM_001351295.1:c.2543G= NP_001338224.1:p.Gly848=
NM_001351296.1:c.2477G= NP_001338225.1:p.Gly826=
NM_001351297.1:c.2474G= NP_001338226.1:p.Gly825=
NR_147094.1:n.2546G=
XM_017018197.2:c.2546G= XP_016873686.1:p.Gly849=
XM_017018199.1:c.2543G= XP_016873688.1:p.Gly848=
XM_017018201.2:c.2546G= XP_016873690.1:p.Gly849=
XM_017018202.1:c.1043G= XP_016873691.1:p.Gly348=
XM_017018204.1:c.434G= XP_016873693.1:p.Gly145=
XM_024448668.1:c.845G= XP_024304436.1:p.Gly282=
XR_001747945.2:n.2618G=
XR_001747946.2:n.2549G=
XR_002957189.1:n.2618G=
NM_000352.6:c.2477G= MANE Select NP_000343.2:p.Gly826=
NM_001287174.2:c.2480G= NP_001274103.1:p.Gly827=
NM_001351295.2:c.2543G= NP_001338224.1:p.Gly848=
NM_001351296.2:c.2477G= NP_001338225.1:p.Gly826=
NM_001351297.2:c.2474G= NP_001338226.1:p.Gly825=
NR_147094.2:n.2546G=
NM_001287174.3:c.2480G= NP_001274103.1:p.Gly827=