Canonical Allele Identifier: CA1955128638
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17406934C= , CM000673.2:g.17406934C= GRCh38
NC_000011.9:g.17428481C= , CM000673.1:g.17428481C= GRCh37
NC_000011.8:g.17385057C= NCBI36
NG_008867.1:g.74969G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.2685G=
ENST00000529967.6:n.1455G=
ENST00000532220.2:n.848G=
ENST00000642611.2:n.3185G=
ENST00000645004.2:n.615G=
ENST00000682051.1:n.3132G=
ENST00000682110.1:n.3185G=
ENST00000682140.1:c.3113G= ENSP00000507829.1:p.Ser1038=
ENST00000682185.1:n.4421G=
ENST00000682204.1:c.*1254G= ENSP00000507094.1:n.*1254G=
ENST00000682215.1:n.3182G=
ENST00000682288.1:c.*1547G= ENSP00000507506.1:n.*1547G=
ENST00000682442.1:n.3306G=
ENST00000682528.1:n.3262G=
ENST00000682673.1:n.3129G=
ENST00000682805.1:n.3182G=
ENST00000682965.1:c.3113G= ENSP00000508229.1:p.Ser1038=
ENST00000683093.1:n.3284G=
ENST00000683136.1:c.3113G= ENSP00000507768.1:p.Ser1038=
ENST00000683153.1:n.3341G=
ENST00000683365.1:n.3287G=
ENST00000683377.1:n.3185G=
ENST00000683456.1:c.*253G= ENSP00000508318.1:n.*253G=
ENST00000683522.1:n.3185G=
ENST00000683562.1:c.*1285G= ENSP00000508265.1:n.*1285G=
ENST00000683693.1:n.3262G=
ENST00000683725.1:c.3116G= ENSP00000507496.1:p.Ser1039=
ENST00000684010.1:n.3180G=
ENST00000684157.1:n.3185G=
ENST00000684253.1:n.3088G=
ENST00000684288.1:c.*1288G= ENSP00000507143.1:n.*1288G=
ENST00000684313.1:n.2617G=
ENST00000684332.1:n.3258G=
ENST00000684371.1:n.3291G=
ENST00000684404.1:n.3228G=
ENST00000684442.1:n.3185G=
ENST00000684555.1:c.*1328G= ENSP00000507705.1:n.*1328G=
ENST00000684571.1:c.2957G= ENSP00000506935.1:p.Ser986=
ENST00000684593.1:c.*2821G= ENSP00000507005.1:n.*2821G=
ENST00000684711.1:c.*1512G= ENSP00000506841.1:n.*1512G=
ENST00000302539.9:c.3119G= ENSP00000303960.4:p.Ser1040=
ENST00000389817.8:c.3116G= MANE Select ENSP00000374467.4:p.Ser1039=
ENST00000642271.1:c.3113G= ENSP00000493749.1:p.Ser1038=
ENST00000642579.1:c.1200G=
ENST00000642611.1:n.3070G=
ENST00000642902.1:c.2898G=
ENST00000643260.1:c.3116G= ENSP00000494450.1:p.Ser1039=
ENST00000643562.1:c.*1092G= ENSP00000496124.1:n.*1092G=
ENST00000643925.1:c.1240G=
ENST00000644447.1:c.1472G= ENSP00000496282.1:p.Ser491=
ENST00000644484.1:c.*1371G= ENSP00000493558.1:n.*1371G=
ENST00000644542.1:c.*2821G= ENSP00000495532.1:n.*2821G=
ENST00000644675.1:c.*1288G= ENSP00000494567.1:n.*1288G=
ENST00000644757.1:c.*1401G= ENSP00000495085.1:n.*1401G=
ENST00000644772.1:c.3182G= ENSP00000494321.1:p.Ser1061=
ENST00000645004.1:n.255G=
ENST00000645076.1:c.2315G=
ENST00000645417.1:c.282G=
ENST00000645744.1:c.*1380G= ENSP00000494564.1:n.*1380G=
ENST00000645760.1:c.3391G=
ENST00000645884.1:c.*253G= ENSP00000495516.1:n.*253G=
ENST00000646003.1:c.*1072G= ENSP00000495259.1:n.*1072G=
ENST00000646207.1:c.*1583G= ENSP00000495025.1:n.*1583G=
ENST00000646276.1:c.*1389G= ENSP00000496070.1:n.*1389G=
ENST00000646592.1:c.2422G=
ENST00000646902.1:c.3113G= ENSP00000494101.1:p.Ser1038=
ENST00000646993.1:c.*1512G= ENSP00000493720.1:n.*1512G=
ENST00000647013.1:c.3122G= ENSP00000496741.1:n.3122G=
ENST00000647015.1:c.2867G= ENSP00000495389.1:p.Ser956=
ENST00000647086.1:c.*2846G= ENSP00000493677.1:n.*2846G=
ENST00000647158.1:c.*1257G= ENSP00000495744.1:n.*1257G=
ENST00000302539.8:c.3119G= ENSP00000303960.4:p.Ser1040=
ENST00000389817.7:c.3116G= ENSP00000374467.3:p.Ser1039=
ENST00000524561.1:n.248G=
ENST00000526921.5:n.800G=
ENST00000527905.5:c.2986G= ENSP00000431653.1:p.Ala996=
ENST00000529967.5:n.785G=
NM_000352.4:c.3116G= NP_000343.2:p.Ser1039=
NM_001287174.1:c.3119G= NP_001274103.1:p.Ser1040=
XM_011520331.1:c.3116G= XP_011518633.1:p.Ser1039=
XM_011520332.1:c.3119G= XP_011518634.1:p.Ser1040=
XM_011520333.1:c.1616G= XP_011518635.1:p.Ser539=
XR_930890.1:n.3182G=
XR_930891.1:n.3182G=
XR_930892.1:n.3082G=
XR_930893.1:n.3079G=
NM_001351295.1:c.3182G= NP_001338224.1:p.Ser1061=
NM_001351296.1:c.3116G= NP_001338225.1:p.Ser1039=
NM_001351297.1:c.3113G= NP_001338226.1:p.Ser1038=
NR_147094.1:n.3265G=
XM_017018197.2:c.3185G= XP_016873686.1:p.Ser1062=
XM_017018199.1:c.3182G= XP_016873688.1:p.Ser1061=
XM_017018201.2:c.3185G= XP_016873690.1:p.Ser1062=
XM_017018202.1:c.1682G= XP_016873691.1:p.Ser561=
XM_017018204.1:c.1073G= XP_016873693.1:p.Ser358=
XM_024448668.1:c.1484G= XP_024304436.1:p.Ser495=
XR_001747945.2:n.3257G=
XR_001747946.2:n.3188G=
XR_002957189.1:n.3337G=
NM_000352.6:c.3116G= MANE Select NP_000343.2:p.Ser1039=
NM_001287174.2:c.3119G= NP_001274103.1:p.Ser1040=
NM_001351295.2:c.3182G= NP_001338224.1:p.Ser1061=
NM_001351296.2:c.3116G= NP_001338225.1:p.Ser1039=
NM_001351297.2:c.3113G= NP_001338226.1:p.Ser1038=
NR_147094.2:n.3265G=
NM_001287174.3:c.3119G= NP_001274103.1:p.Ser1040=