Canonical Allele Identifier: CA1955122587
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17394360C= , CM000673.2:g.17394360C= GRCh38
NC_000011.9:g.17415907C= , CM000673.1:g.17415907C= GRCh37
NC_000011.8:g.17372483C= NCBI36
NG_008867.1:g.87543G=

Transcript Alleles

HGVS Amino-acid change
ENST00000524561.2:n.4052G=
ENST00000526037.6:n.386G=
ENST00000528374.2:c.1042G=
ENST00000529967.6:n.2790G=
ENST00000532220.2:n.3684G=
ENST00000642611.2:n.5784G=
ENST00000644057.2:n.1027G=
ENST00000645004.2:n.1950G=
ENST00000682051.1:n.4613G=
ENST00000682110.1:n.4666G=
ENST00000682140.1:c.*237G= ENSP00000507829.1:n.*237G=
ENST00000682185.1:n.5756G=
ENST00000682204.1:c.*2589G= ENSP00000507094.1:n.*2589G=
ENST00000682215.1:n.5033G=
ENST00000682288.1:c.*2882G= ENSP00000507506.1:n.*2882G=
ENST00000682442.1:n.4886G=
ENST00000682528.1:n.4743G=
ENST00000682673.1:n.4610G=
ENST00000682805.1:n.5071G=
ENST00000682965.1:c.*873G= ENSP00000508229.1:n.*873G=
ENST00000683093.1:n.5646G=
ENST00000683136.1:c.4334G= ENSP00000507768.1:p.Gly1445=
ENST00000683153.1:n.4708G=
ENST00000683365.1:n.4768G=
ENST00000683377.1:n.4562G=
ENST00000683456.1:c.*1588G= ENSP00000508318.1:n.*1588G=
ENST00000683522.1:n.4748G=
ENST00000683562.1:c.*2516G= ENSP00000508265.1:n.*2516G=
ENST00000683693.1:n.6127G=
ENST00000683725.1:c.4347G= ENSP00000507496.1:p.Gly1449=
ENST00000684010.1:n.4661G=
ENST00000684014.1:n.638G=
ENST00000684157.1:n.5651G=
ENST00000684253.1:n.4569G=
ENST00000684288.1:c.*2623G= ENSP00000507143.1:n.*2623G=
ENST00000684313.1:n.4098G=
ENST00000684332.1:n.4739G=
ENST00000684371.1:n.4772G=
ENST00000684404.1:n.5694G=
ENST00000684442.1:n.4890G=
ENST00000684555.1:c.*2663G= ENSP00000507705.1:n.*2663G=
ENST00000684571.1:c.4292G= ENSP00000506935.1:p.Gly1431=
ENST00000684593.1:c.*4156G= ENSP00000507005.1:n.*4156G=
ENST00000684711.1:c.*2847G= ENSP00000506841.1:n.*2847G=
ENST00000302539.9:c.4454G= ENSP00000303960.4:p.Gly1485=
ENST00000389817.8:c.4451G= MANE Select ENSP00000374467.4:p.Gly1484=
ENST00000642271.1:c.4448G= ENSP00000493749.1:p.Gly1483=
ENST00000642579.1:c.2505G=
ENST00000642611.1:n.5669G=
ENST00000642902.1:c.4233G=
ENST00000643260.1:c.4451G= ENSP00000494450.1:p.Gly1484=
ENST00000643562.1:c.*2573G= ENSP00000496124.1:n.*2573G=
ENST00000643925.1:c.3091G=
ENST00000644057.1:n.610G=
ENST00000644484.1:c.*3837G= ENSP00000493558.1:n.*3837G=
ENST00000644675.1:c.*2623G= ENSP00000494567.1:n.*2623G=
ENST00000644757.1:c.*3203-1380G= ENSP00000495085.1:n.*3203-1380G=
ENST00000644772.1:c.4517G= ENSP00000494321.1:p.Gly1506=
ENST00000645004.1:n.2144G=
ENST00000645076.1:c.3546G=
ENST00000645417.1:c.1639G=
ENST00000645744.1:c.*4136G= ENSP00000494564.1:n.*4136G=
ENST00000645760.1:c.4872G=
ENST00000645884.1:c.*1734G= ENSP00000495516.1:n.*1734G=
ENST00000646003.1:c.*2473G= ENSP00000495259.1:n.*2473G=
ENST00000646207.1:c.*3288G= ENSP00000495025.1:n.*3288G=
ENST00000646276.1:c.*3855G= ENSP00000496070.1:n.*3855G=
ENST00000646592.1:c.3757G=
ENST00000646902.1:c.4418G= ENSP00000494101.1:p.Gly1473=
ENST00000646993.1:c.*2889G= ENSP00000493720.1:n.*2889G=
ENST00000647013.1:c.4457G= ENSP00000496741.1:n.4457G=
ENST00000647015.1:c.4202G= ENSP00000495389.1:p.Gly1401=
ENST00000647086.1:c.*4037G= ENSP00000493677.1:n.*4037G=
ENST00000647158.1:c.*2738G= ENSP00000495744.1:n.*2738G=
ENST00000302539.8:c.4454G= ENSP00000303960.4:p.Gly1485=
ENST00000389817.7:c.4451G= ENSP00000374467.3:p.Gly1484=
ENST00000525022.1:n.346G=
ENST00000526037.5:n.211G=
ENST00000526168.5:c.239G=
ENST00000531642.5:c.482G=
NM_000352.4:c.4451G= NP_000343.2:p.Gly1484=
NM_001287174.1:c.4454G= NP_001274103.1:p.Gly1485=
XM_011520331.1:c.4451G= XP_011518633.1:p.Gly1484=
XM_011520332.1:c.4350G= XP_011518634.1:p.Gly1450=
XM_011520333.1:c.2951G= XP_011518635.1:p.Gly984=
XR_930890.1:n.4413G=
NM_001351295.1:c.4517G= NP_001338224.1:p.Gly1506=
NM_001351296.1:c.4451G= NP_001338225.1:p.Gly1484=
NM_001351297.1:c.4448G= NP_001338226.1:p.Gly1483=
NR_147094.1:n.4746G=
XM_017018197.2:c.4520G= XP_016873686.1:p.Gly1507=
XM_017018199.1:c.4517G= XP_016873688.1:p.Gly1506=
XM_017018201.2:c.4416G= XP_016873690.1:p.Gly1472=
XM_017018202.1:c.3017G= XP_016873691.1:p.Gly1006=
XM_017018204.1:c.2408G= XP_016873693.1:p.Gly803=
XM_024448668.1:c.2819G= XP_024304436.1:p.Gly940=
XR_001747945.2:n.4488G=
XR_001747946.2:n.4419G=
XR_002957189.1:n.6202G=
NM_000352.6:c.4451G= MANE Select NP_000343.2:p.Gly1484=
NM_001287174.2:c.4454G= NP_001274103.1:p.Gly1485=
NM_001351295.2:c.4517G= NP_001338224.1:p.Gly1506=
NM_001351296.2:c.4451G= NP_001338225.1:p.Gly1484=
NM_001351297.2:c.4448G= NP_001338226.1:p.Gly1483=
NR_147094.2:n.4746G=
NM_001287174.3:c.4454G= NP_001274103.1:p.Gly1485=