Canonical Allele Identifier: CA2574768411
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17406827C>A , CM000673.2:g.17406827C>A GRCh38
NC_000011.9:g.17428374C>A , CM000673.1:g.17428374C>A GRCh37
NC_000011.8:g.17384950C>A NCBI36
NG_008867.1:g.75076G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.2732-39G>T
ENST00000529967.6:n.1502-39G>T
ENST00000532220.2:n.895-39G>T
ENST00000642611.2:n.3232-39G>T
ENST00000645004.2:n.662-39G>T
ENST00000682051.1:n.3179-39G>T
ENST00000682110.1:n.3232-39G>T
ENST00000682140.1:c.3160-39G>T ENSP00000507829.1:n.3160-39G>T
ENST00000682185.1:n.4468-39G>T
ENST00000682204.1:c.*1301-39G>T ENSP00000507094.1:n.*1301-39G>T
ENST00000682215.1:n.3229-39G>T
ENST00000682288.1:c.*1594-39G>T ENSP00000507506.1:n.*1594-39G>T
ENST00000682442.1:n.3413G>T
ENST00000682528.1:n.3309-39G>T
ENST00000682673.1:n.3176-39G>T
ENST00000682805.1:n.3229-39G>T
ENST00000682965.1:c.3160-39G>T ENSP00000508229.1:n.3160-39G>T
ENST00000683093.1:n.3331-39G>T
ENST00000683136.1:c.3160-39G>T ENSP00000507768.1:n.3160-39G>T
ENST00000683153.1:n.3388-39G>T
ENST00000683365.1:n.3334-39G>T
ENST00000683377.1:n.3232-39G>T
ENST00000683456.1:c.*300-39G>T ENSP00000508318.1:n.*300-39G>T
ENST00000683522.1:n.3232-39G>T
ENST00000683562.1:c.*1332-39G>T ENSP00000508265.1:n.*1332-39G>T
ENST00000683693.1:n.3309-39G>T
ENST00000683725.1:c.3163-39G>T ENSP00000507496.1:n.3163-39G>T
ENST00000684010.1:n.3227-39G>T
ENST00000684157.1:n.3232-39G>T
ENST00000684253.1:n.3135-39G>T
ENST00000684288.1:c.*1335-39G>T ENSP00000507143.1:n.*1335-39G>T
ENST00000684313.1:n.2664-39G>T
ENST00000684332.1:n.3305-39G>T
ENST00000684371.1:n.3338-39G>T
ENST00000684404.1:n.3275-39G>T
ENST00000684442.1:n.3232-39G>T
ENST00000684555.1:c.*1375-39G>T ENSP00000507705.1:n.*1375-39G>T
ENST00000684571.1:c.3004-39G>T ENSP00000506935.1:n.3004-39G>T
ENST00000684593.1:c.*2868-39G>T ENSP00000507005.1:n.*2868-39G>T
ENST00000684711.1:c.*1559-39G>T ENSP00000506841.1:n.*1559-39G>T
ENST00000302539.9:c.3166-39G>T ENSP00000303960.4:n.3166-39G>T
ENST00000389817.8:c.3163-39G>T MANE Select ENSP00000374467.4:n.3163-39G>T
ENST00000642271.1:c.3160-39G>T ENSP00000493749.1:n.3160-39G>T
ENST00000642579.1:c.1247-39G>T
ENST00000642611.1:n.3117-39G>T
ENST00000642902.1:c.2945-39G>T
ENST00000643260.1:c.3163-39G>T ENSP00000494450.1:n.3163-39G>T
ENST00000643562.1:c.*1139-39G>T ENSP00000496124.1:n.*1139-39G>T
ENST00000643925.1:c.1287-39G>T
ENST00000644447.1:c.1519-39G>T ENSP00000496282.1:n.1519-39G>T
ENST00000644484.1:c.*1418-39G>T ENSP00000493558.1:n.*1418-39G>T
ENST00000644542.1:c.*2928G>T ENSP00000495532.1:n.*2928G>T
ENST00000644675.1:c.*1335-39G>T ENSP00000494567.1:n.*1335-39G>T
ENST00000644757.1:c.*1448-39G>T ENSP00000495085.1:n.*1448-39G>T
ENST00000644772.1:c.3229-39G>T ENSP00000494321.1:n.3229-39G>T
ENST00000645004.1:n.302-39G>T
ENST00000645076.1:c.2362-39G>T
ENST00000645417.1:c.329-39G>T
ENST00000645744.1:c.*1427-39G>T ENSP00000494564.1:n.*1427-39G>T
ENST00000645760.1:c.3438-39G>T
ENST00000645884.1:c.*300-39G>T ENSP00000495516.1:n.*300-39G>T
ENST00000646003.1:c.*1119-39G>T ENSP00000495259.1:n.*1119-39G>T
ENST00000646207.1:c.*1630-39G>T ENSP00000495025.1:n.*1630-39G>T
ENST00000646276.1:c.*1436-39G>T ENSP00000496070.1:n.*1436-39G>T
ENST00000646592.1:c.2469-39G>T
ENST00000646902.1:c.3160-39G>T ENSP00000494101.1:n.3160-39G>T
ENST00000646993.1:c.*1559-39G>T ENSP00000493720.1:n.*1559-39G>T
ENST00000647013.1:c.3169-39G>T ENSP00000496741.1:n.3169-39G>T
ENST00000647015.1:c.2914-39G>T ENSP00000495389.1:n.2914-39G>T
ENST00000647086.1:c.*2893-39G>T ENSP00000493677.1:n.*2893-39G>T
ENST00000647158.1:c.*1304-39G>T ENSP00000495744.1:n.*1304-39G>T
ENST00000302539.8:c.3166-39G>T ENSP00000303960.4:n.3166-39G>T
ENST00000389817.7:c.3163-39G>T ENSP00000374467.3:n.3163-39G>T
ENST00000524561.1:n.295-39G>T
ENST00000526921.5:n.847-39G>T
ENST00000527905.5:c.*39-39G>T ENSP00000431653.1:n.*39-39G>T
NM_000352.4:c.3163-39G>T NP_000343.2:n.3163-39G>T
NM_001287174.1:c.3166-39G>T NP_001274103.1:n.3166-39G>T
XM_011520331.1:c.3163-39G>T XP_011518633.1:n.3163-39G>T
XM_011520332.1:c.3166-39G>T XP_011518634.1:n.3166-39G>T
XM_011520333.1:c.1663-39G>T XP_011518635.1:n.1663-39G>T
XR_930890.1:n.3229-39G>T
XR_930891.1:n.3229-39G>T
XR_930892.1:n.3129-39G>T
XR_930893.1:n.3126-39G>T
NM_001351295.1:c.3229-39G>T NP_001338224.1:n.3229-39G>T
NM_001351296.1:c.3163-39G>T NP_001338225.1:n.3163-39G>T
NM_001351297.1:c.3160-39G>T NP_001338226.1:n.3160-39G>T
NR_147094.1:n.3312-39G>T
XM_017018197.2:c.3232-39G>T XP_016873686.1:n.3232-39G>T
XM_017018199.1:c.3229-39G>T XP_016873688.1:n.3229-39G>T
XM_017018201.2:c.3232-39G>T XP_016873690.1:n.3232-39G>T
XM_017018202.1:c.1729-39G>T XP_016873691.1:n.1729-39G>T
XM_017018204.1:c.1120-39G>T XP_016873693.1:n.1120-39G>T
XM_024448668.1:c.1531-39G>T XP_024304436.1:n.1531-39G>T
XR_001747945.2:n.3304-39G>T
XR_001747946.2:n.3235-39G>T
XR_002957189.1:n.3384-39G>T
NM_000352.6:c.3163-39G>T MANE Select NP_000343.2:n.3163-39G>T
NM_001287174.2:c.3166-39G>T NP_001274103.1:n.3166-39G>T
NM_001351295.2:c.3229-39G>T NP_001338224.1:n.3229-39G>T
NM_001351296.2:c.3163-39G>T NP_001338225.1:n.3163-39G>T
NM_001351297.2:c.3160-39G>T NP_001338226.1:n.3160-39G>T
NR_147094.2:n.3312-39G>T
NM_001287174.3:c.3166-39G>T NP_001274103.1:n.3166-39G>T