Canonical Allele Identifier: CA1955123373
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17395925C= , CM000673.2:g.17395925C= GRCh38
NC_000011.9:g.17417472C= , CM000673.1:g.17417472C= GRCh37
NC_000011.8:g.17374048C= NCBI36
NG_008867.1:g.85978G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.3726G=
ENST00000528374.2:c.716G=
ENST00000529967.6:n.2464G=
ENST00000532220.2:n.3358G=
ENST00000642611.2:n.5325G=
ENST00000644057.2:n.568G=
ENST00000645004.2:n.1624G=
ENST00000682051.1:n.4287G=
ENST00000682110.1:n.4340G=
ENST00000682140.1:c.3991G= ENSP00000507829.1:p.Asp1331=
ENST00000682185.1:n.5430G=
ENST00000682204.1:c.*2263G= ENSP00000507094.1:n.*2263G=
ENST00000682215.1:n.4707G=
ENST00000682288.1:c.*2556G= ENSP00000507506.1:n.*2556G=
ENST00000682442.1:n.4560G=
ENST00000682528.1:n.4417G=
ENST00000682673.1:n.4284G=
ENST00000682805.1:n.4745G=
ENST00000682965.1:c.*547G= ENSP00000508229.1:n.*547G=
ENST00000683093.1:n.5424G=
ENST00000683136.1:c.4008G= ENSP00000507768.1:p.Gly1336=
ENST00000683153.1:n.4382G=
ENST00000683365.1:n.4442G=
ENST00000683377.1:n.4340G=
ENST00000683456.1:c.*1262G= ENSP00000508318.1:n.*1262G=
ENST00000683522.1:n.4340G=
ENST00000683562.1:c.*2294G= ENSP00000508265.1:n.*2294G=
ENST00000683693.1:n.5772G=
ENST00000683725.1:c.4125G= ENSP00000507496.1:p.Gly1375=
ENST00000684010.1:n.4335G=
ENST00000684157.1:n.5325G=
ENST00000684253.1:n.4243G=
ENST00000684288.1:c.*2297G= ENSP00000507143.1:n.*2297G=
ENST00000684313.1:n.3772G=
ENST00000684332.1:n.4413G=
ENST00000684371.1:n.4446G=
ENST00000684404.1:n.5368G=
ENST00000684442.1:n.4564G=
ENST00000684555.1:c.*2337G= ENSP00000507705.1:n.*2337G=
ENST00000684571.1:c.3966G= ENSP00000506935.1:p.Gly1322=
ENST00000684593.1:c.*3830G= ENSP00000507005.1:n.*3830G=
ENST00000684711.1:c.*2521G= ENSP00000506841.1:n.*2521G=
ENST00000302539.9:c.4128G= ENSP00000303960.4:p.Gly1376=
ENST00000389817.8:c.4125G= MANE Select ENSP00000374467.4:p.Gly1375=
ENST00000642271.1:c.4122G= ENSP00000493749.1:p.Gly1374=
ENST00000642579.1:c.2179G=
ENST00000642611.1:n.5210G=
ENST00000642902.1:c.3907G=
ENST00000643260.1:c.4125G= ENSP00000494450.1:p.Gly1375=
ENST00000643562.1:c.*2247G= ENSP00000496124.1:n.*2247G=
ENST00000643925.1:c.2765G=
ENST00000644057.1:n.202G=
ENST00000644484.1:c.*3511G= ENSP00000493558.1:n.*3511G=
ENST00000644675.1:c.*2297G= ENSP00000494567.1:n.*2297G=
ENST00000644757.1:c.*3202+339G= ENSP00000495085.1:n.*3202+339G=
ENST00000644772.1:c.4191G= ENSP00000494321.1:p.Gly1397=
ENST00000645004.1:n.1818G=
ENST00000645076.1:c.3324G=
ENST00000645417.1:c.1313G=
ENST00000645744.1:c.*3890G= ENSP00000494564.1:n.*3890G=
ENST00000645760.1:c.4546G=
ENST00000645884.1:c.*1408G= ENSP00000495516.1:n.*1408G=
ENST00000646003.1:c.*2227G= ENSP00000495259.1:n.*2227G=
ENST00000646207.1:c.*2962G= ENSP00000495025.1:n.*2962G=
ENST00000646276.1:c.*3529G= ENSP00000496070.1:n.*3529G=
ENST00000646592.1:c.3431G=
ENST00000646902.1:c.4092G= ENSP00000494101.1:p.Gly1364=
ENST00000646993.1:c.*2667G= ENSP00000493720.1:n.*2667G=
ENST00000647013.1:c.4131G= ENSP00000496741.1:n.4131G=
ENST00000647015.1:c.3876G= ENSP00000495389.1:p.Gly1292=
ENST00000647086.1:c.*3711G= ENSP00000493677.1:n.*3711G=
ENST00000647158.1:c.*2412G= ENSP00000495744.1:n.*2412G=
ENST00000302539.8:c.4128G= ENSP00000303960.4:p.Gly1376=
ENST00000389817.7:c.4125G= ENSP00000374467.3:p.Gly1375=
ENST00000528374.1:c.607G=
ENST00000532220.1:n.599G=
NM_000352.4:c.4125G= NP_000343.2:p.Gly1375=
NM_001287174.1:c.4128G= NP_001274103.1:p.Gly1376=
XM_011520331.1:c.4125G= XP_011518633.1:p.Gly1375=
XM_011520332.1:c.4128G= XP_011518634.1:p.Gly1376=
XM_011520333.1:c.2625G= XP_011518635.1:p.Gly875=
XR_930890.1:n.4191G=
NM_001351295.1:c.4191G= NP_001338224.1:p.Gly1397=
NM_001351296.1:c.4125G= NP_001338225.1:p.Gly1375=
NM_001351297.1:c.4122G= NP_001338226.1:p.Gly1374=
NR_147094.1:n.4420G=
XM_017018197.2:c.4194G= XP_016873686.1:p.Gly1398=
XM_017018199.1:c.4191G= XP_016873688.1:p.Gly1397=
XM_017018201.2:c.4194G= XP_016873690.1:p.Gly1398=
XM_017018202.1:c.2691G= XP_016873691.1:p.Gly897=
XM_017018204.1:c.2082G= XP_016873693.1:p.Gly694=
XM_024448668.1:c.2493G= XP_024304436.1:p.Gly831=
XR_001747945.2:n.4266G=
XR_001747946.2:n.4197G=
XR_002957189.1:n.5847G=
NM_000352.6:c.4125G= MANE Select NP_000343.2:p.Gly1375=
NM_001287174.2:c.4128G= NP_001274103.1:p.Gly1376=
NM_001351295.2:c.4191G= NP_001338224.1:p.Gly1397=
NM_001351296.2:c.4125G= NP_001338225.1:p.Gly1375=
NM_001351297.2:c.4122G= NP_001338226.1:p.Gly1374=
NR_147094.2:n.4420G=
NM_001287174.3:c.4128G= NP_001274103.1:p.Gly1376=