Canonical Allele Identifier: CA1955128655
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17406968C= , CM000673.2:g.17406968C= GRCh38
NC_000011.9:g.17428515C= , CM000673.1:g.17428515C= GRCh37
NC_000011.8:g.17385091C= NCBI36
NG_008867.1:g.74935G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.2651G=
ENST00000529967.6:n.1421G=
ENST00000532220.2:n.814G=
ENST00000642611.2:n.3151G=
ENST00000645004.2:n.581G=
ENST00000682051.1:n.3098G=
ENST00000682110.1:n.3151G=
ENST00000682140.1:c.3079G= ENSP00000507829.1:p.Ala1027=
ENST00000682185.1:n.4387G=
ENST00000682204.1:c.*1220G= ENSP00000507094.1:n.*1220G=
ENST00000682215.1:n.3148G=
ENST00000682288.1:c.*1513G= ENSP00000507506.1:n.*1513G=
ENST00000682442.1:n.3272G=
ENST00000682528.1:n.3228G=
ENST00000682673.1:n.3095G=
ENST00000682805.1:n.3148G=
ENST00000682965.1:c.3079G= ENSP00000508229.1:p.Ala1027=
ENST00000683093.1:n.3250G=
ENST00000683136.1:c.3079G= ENSP00000507768.1:p.Ala1027=
ENST00000683153.1:n.3307G=
ENST00000683365.1:n.3253G=
ENST00000683377.1:n.3151G=
ENST00000683456.1:c.*219G= ENSP00000508318.1:n.*219G=
ENST00000683522.1:n.3151G=
ENST00000683562.1:c.*1251G= ENSP00000508265.1:n.*1251G=
ENST00000683693.1:n.3228G=
ENST00000683725.1:c.3082G= ENSP00000507496.1:p.Ala1028=
ENST00000684010.1:n.3146G=
ENST00000684157.1:n.3151G=
ENST00000684253.1:n.3054G=
ENST00000684288.1:c.*1254G= ENSP00000507143.1:n.*1254G=
ENST00000684313.1:n.2583G=
ENST00000684332.1:n.3224G=
ENST00000684371.1:n.3257G=
ENST00000684404.1:n.3194G=
ENST00000684442.1:n.3151G=
ENST00000684555.1:c.*1294G= ENSP00000507705.1:n.*1294G=
ENST00000684571.1:c.2923G= ENSP00000506935.1:p.Ala975=
ENST00000684593.1:c.*2787G= ENSP00000507005.1:n.*2787G=
ENST00000684711.1:c.*1478G= ENSP00000506841.1:n.*1478G=
ENST00000302539.9:c.3085G= ENSP00000303960.4:p.Ala1029=
ENST00000389817.8:c.3082G= MANE Select ENSP00000374467.4:p.Ala1028=
ENST00000642271.1:c.3079G= ENSP00000493749.1:p.Ala1027=
ENST00000642579.1:c.1166G=
ENST00000642611.1:n.3036G=
ENST00000642902.1:c.2864G=
ENST00000643260.1:c.3082G= ENSP00000494450.1:p.Ala1028=
ENST00000643562.1:c.*1058G= ENSP00000496124.1:n.*1058G=
ENST00000643925.1:c.1206G=
ENST00000644447.1:c.1438G= ENSP00000496282.1:p.Ala480=
ENST00000644484.1:c.*1337G= ENSP00000493558.1:n.*1337G=
ENST00000644542.1:c.*2787G= ENSP00000495532.1:n.*2787G=
ENST00000644675.1:c.*1254G= ENSP00000494567.1:n.*1254G=
ENST00000644757.1:c.*1367G= ENSP00000495085.1:n.*1367G=
ENST00000644772.1:c.3148G= ENSP00000494321.1:p.Ala1050=
ENST00000645004.1:n.221G=
ENST00000645076.1:c.2281G=
ENST00000645417.1:c.248G=
ENST00000645744.1:c.*1346G= ENSP00000494564.1:n.*1346G=
ENST00000645760.1:c.3357G=
ENST00000645884.1:c.*219G= ENSP00000495516.1:n.*219G=
ENST00000646003.1:c.*1038G= ENSP00000495259.1:n.*1038G=
ENST00000646207.1:c.*1549G= ENSP00000495025.1:n.*1549G=
ENST00000646276.1:c.*1355G= ENSP00000496070.1:n.*1355G=
ENST00000646592.1:c.2388G=
ENST00000646902.1:c.3079G= ENSP00000494101.1:p.Ala1027=
ENST00000646993.1:c.*1478G= ENSP00000493720.1:n.*1478G=
ENST00000647013.1:c.3088G= ENSP00000496741.1:n.3088G=
ENST00000647015.1:c.2833G= ENSP00000495389.1:p.Ala945=
ENST00000647086.1:c.*2812G= ENSP00000493677.1:n.*2812G=
ENST00000647158.1:c.*1223G= ENSP00000495744.1:n.*1223G=
ENST00000302539.8:c.3085G= ENSP00000303960.4:p.Ala1029=
ENST00000389817.7:c.3082G= ENSP00000374467.3:p.Ala1028=
ENST00000524561.1:n.214G=
ENST00000526921.5:n.766G=
ENST00000527905.5:c.2952G= ENSP00000431653.1:p.Trp984=
ENST00000529967.5:n.751G=
NM_000352.4:c.3082G= NP_000343.2:p.Ala1028=
NM_001287174.1:c.3085G= NP_001274103.1:p.Ala1029=
XM_011520331.1:c.3082G= XP_011518633.1:p.Ala1028=
XM_011520332.1:c.3085G= XP_011518634.1:p.Ala1029=
XM_011520333.1:c.1582G= XP_011518635.1:p.Ala528=
XR_930890.1:n.3148G=
XR_930891.1:n.3148G=
XR_930892.1:n.3048G=
XR_930893.1:n.3045G=
NM_001351295.1:c.3148G= NP_001338224.1:p.Ala1050=
NM_001351296.1:c.3082G= NP_001338225.1:p.Ala1028=
NM_001351297.1:c.3079G= NP_001338226.1:p.Ala1027=
NR_147094.1:n.3231G=
XM_017018197.2:c.3151G= XP_016873686.1:p.Ala1051=
XM_017018199.1:c.3148G= XP_016873688.1:p.Ala1050=
XM_017018201.2:c.3151G= XP_016873690.1:p.Ala1051=
XM_017018202.1:c.1648G= XP_016873691.1:p.Ala550=
XM_017018204.1:c.1039G= XP_016873693.1:p.Ala347=
XM_024448668.1:c.1450G= XP_024304436.1:p.Ala484=
XR_001747945.2:n.3223G=
XR_001747946.2:n.3154G=
XR_002957189.1:n.3303G=
NM_000352.6:c.3082G= MANE Select NP_000343.2:p.Ala1028=
NM_001287174.2:c.3085G= NP_001274103.1:p.Ala1029=
NM_001351295.2:c.3148G= NP_001338224.1:p.Ala1050=
NM_001351296.2:c.3082G= NP_001338225.1:p.Ala1028=
NM_001351297.2:c.3079G= NP_001338226.1:p.Ala1027=
NR_147094.2:n.3231G=
NM_001287174.3:c.3085G= NP_001274103.1:p.Ala1029=