Canonical Allele Identifier: CA1955123364
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17395909C= , CM000673.2:g.17395909C= GRCh38
NC_000011.9:g.17417456C= , CM000673.1:g.17417456C= GRCh37
NC_000011.8:g.17374032C= NCBI36
NG_008867.1:g.85994G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.3742G=
ENST00000528374.2:c.732G=
ENST00000529967.6:n.2480G=
ENST00000532220.2:n.3374G=
ENST00000642611.2:n.5341G=
ENST00000644057.2:n.584G=
ENST00000645004.2:n.1640G=
ENST00000682051.1:n.4303G=
ENST00000682110.1:n.4356G=
ENST00000682140.1:c.4007G= ENSP00000507829.1:p.Arg1336=
ENST00000682185.1:n.5446G=
ENST00000682204.1:c.*2279G= ENSP00000507094.1:n.*2279G=
ENST00000682215.1:n.4723G=
ENST00000682288.1:c.*2572G= ENSP00000507506.1:n.*2572G=
ENST00000682442.1:n.4576G=
ENST00000682528.1:n.4433G=
ENST00000682673.1:n.4300G=
ENST00000682805.1:n.4761G=
ENST00000682965.1:c.*563G= ENSP00000508229.1:n.*563G=
ENST00000683093.1:n.5440G=
ENST00000683136.1:c.4024G= ENSP00000507768.1:p.Gly1342=
ENST00000683153.1:n.4398G=
ENST00000683365.1:n.4458G=
ENST00000683377.1:n.4356G=
ENST00000683456.1:c.*1278G= ENSP00000508318.1:n.*1278G=
ENST00000683522.1:n.4356G=
ENST00000683562.1:c.*2310G= ENSP00000508265.1:n.*2310G=
ENST00000683693.1:n.5788G=
ENST00000683725.1:c.4141G= ENSP00000507496.1:p.Gly1381=
ENST00000684010.1:n.4351G=
ENST00000684157.1:n.5341G=
ENST00000684253.1:n.4259G=
ENST00000684288.1:c.*2313G= ENSP00000507143.1:n.*2313G=
ENST00000684313.1:n.3788G=
ENST00000684332.1:n.4429G=
ENST00000684371.1:n.4462G=
ENST00000684404.1:n.5384G=
ENST00000684442.1:n.4580G=
ENST00000684555.1:c.*2353G= ENSP00000507705.1:n.*2353G=
ENST00000684571.1:c.3982G= ENSP00000506935.1:p.Gly1328=
ENST00000684593.1:c.*3846G= ENSP00000507005.1:n.*3846G=
ENST00000684711.1:c.*2537G= ENSP00000506841.1:n.*2537G=
ENST00000302539.9:c.4144G= ENSP00000303960.4:p.Gly1382=
ENST00000389817.8:c.4141G= MANE Select ENSP00000374467.4:p.Gly1381=
ENST00000642271.1:c.4138G= ENSP00000493749.1:p.Gly1380=
ENST00000642579.1:c.2195G=
ENST00000642611.1:n.5226G=
ENST00000642902.1:c.3923G=
ENST00000643260.1:c.4141G= ENSP00000494450.1:p.Gly1381=
ENST00000643562.1:c.*2263G= ENSP00000496124.1:n.*2263G=
ENST00000643925.1:c.2781G=
ENST00000644057.1:n.218G=
ENST00000644484.1:c.*3527G= ENSP00000493558.1:n.*3527G=
ENST00000644675.1:c.*2313G= ENSP00000494567.1:n.*2313G=
ENST00000644757.1:c.*3202+355G= ENSP00000495085.1:n.*3202+355G=
ENST00000644772.1:c.4207G= ENSP00000494321.1:p.Gly1403=
ENST00000645004.1:n.1834G=
ENST00000645076.1:c.3340G=
ENST00000645417.1:c.1329G=
ENST00000645744.1:c.*3906G= ENSP00000494564.1:n.*3906G=
ENST00000645760.1:c.4562G=
ENST00000645884.1:c.*1424G= ENSP00000495516.1:n.*1424G=
ENST00000646003.1:c.*2243G= ENSP00000495259.1:n.*2243G=
ENST00000646207.1:c.*2978G= ENSP00000495025.1:n.*2978G=
ENST00000646276.1:c.*3545G= ENSP00000496070.1:n.*3545G=
ENST00000646592.1:c.3447G=
ENST00000646902.1:c.4108G= ENSP00000494101.1:p.Gly1370=
ENST00000646993.1:c.*2683G= ENSP00000493720.1:n.*2683G=
ENST00000647013.1:c.4147G= ENSP00000496741.1:n.4147G=
ENST00000647015.1:c.3892G= ENSP00000495389.1:p.Gly1298=
ENST00000647086.1:c.*3727G= ENSP00000493677.1:n.*3727G=
ENST00000647158.1:c.*2428G= ENSP00000495744.1:n.*2428G=
ENST00000302539.8:c.4144G= ENSP00000303960.4:p.Gly1382=
ENST00000389817.7:c.4141G= ENSP00000374467.3:p.Gly1381=
ENST00000525022.1:n.7G=
ENST00000526168.5:c.9G=
NM_000352.4:c.4141G= NP_000343.2:p.Gly1381=
NM_001287174.1:c.4144G= NP_001274103.1:p.Gly1382=
XM_011520331.1:c.4141G= XP_011518633.1:p.Gly1381=
XM_011520332.1:c.4144G= XP_011518634.1:p.Gly1382=
XM_011520333.1:c.2641G= XP_011518635.1:p.Gly881=
XR_930890.1:n.4207G=
NM_001351295.1:c.4207G= NP_001338224.1:p.Gly1403=
NM_001351296.1:c.4141G= NP_001338225.1:p.Gly1381=
NM_001351297.1:c.4138G= NP_001338226.1:p.Gly1380=
NR_147094.1:n.4436G=
XM_017018197.2:c.4210G= XP_016873686.1:p.Gly1404=
XM_017018199.1:c.4207G= XP_016873688.1:p.Gly1403=
XM_017018201.2:c.4210G= XP_016873690.1:p.Gly1404=
XM_017018202.1:c.2707G= XP_016873691.1:p.Gly903=
XM_017018204.1:c.2098G= XP_016873693.1:p.Gly700=
XM_024448668.1:c.2509G= XP_024304436.1:p.Gly837=
XR_001747945.2:n.4282G=
XR_001747946.2:n.4213G=
XR_002957189.1:n.5863G=
NM_000352.6:c.4141G= MANE Select NP_000343.2:p.Gly1381=
NM_001287174.2:c.4144G= NP_001274103.1:p.Gly1382=
NM_001351295.2:c.4207G= NP_001338224.1:p.Gly1403=
NM_001351296.2:c.4141G= NP_001338225.1:p.Gly1381=
NM_001351297.2:c.4138G= NP_001338226.1:p.Gly1380=
NR_147094.2:n.4436G=
NM_001287174.3:c.4144G= NP_001274103.1:p.Gly1382=