Canonical Allele Identifier: CA1955127603
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17404609C= , CM000673.2:g.17404609C= GRCh38
NC_000011.9:g.17426156C= , CM000673.1:g.17426156C= GRCh37
NC_000011.8:g.17382732C= NCBI36
NG_008867.1:g.77294G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.3029G=
ENST00000528374.2:c.39G=
ENST00000529967.6:n.1799G=
ENST00000532220.2:n.1192G=
ENST00000642611.2:n.3529G=
ENST00000645004.2:n.959G=
ENST00000682051.1:n.3476G=
ENST00000682110.1:n.3529G=
ENST00000682140.1:c.3457G= ENSP00000507829.1:p.Ala1153=
ENST00000682185.1:n.4765G=
ENST00000682204.1:c.*1598G= ENSP00000507094.1:n.*1598G=
ENST00000682215.1:n.3526G=
ENST00000682288.1:c.*1891G= ENSP00000507506.1:n.*1891G=
ENST00000682442.1:n.3749G=
ENST00000682528.1:n.3606G=
ENST00000682673.1:n.3473G=
ENST00000682805.1:n.3526G=
ENST00000682965.1:c.3396+885G= ENSP00000508229.1:n.3396+885G=
ENST00000683093.1:n.3628G=
ENST00000683136.1:c.3457G= ENSP00000507768.1:p.Ala1153=
ENST00000683153.1:n.3685G=
ENST00000683365.1:n.3631G=
ENST00000683377.1:n.3529G=
ENST00000683456.1:c.*597G= ENSP00000508318.1:n.*597G=
ENST00000683522.1:n.3529G=
ENST00000683562.1:c.*1629G= ENSP00000508265.1:n.*1629G=
ENST00000683693.1:n.3606G=
ENST00000683725.1:c.3460G= ENSP00000507496.1:p.Ala1154=
ENST00000684010.1:n.3524G=
ENST00000684157.1:n.3529G=
ENST00000684253.1:n.3432G=
ENST00000684288.1:c.*1632G= ENSP00000507143.1:n.*1632G=
ENST00000684313.1:n.2961G=
ENST00000684332.1:n.3602G=
ENST00000684371.1:n.3635G=
ENST00000684404.1:n.3572G=
ENST00000684442.1:n.3529G=
ENST00000684555.1:c.*1672G= ENSP00000507705.1:n.*1672G=
ENST00000684571.1:c.3301G= ENSP00000506935.1:p.Ala1101=
ENST00000684593.1:c.*3165G= ENSP00000507005.1:n.*3165G=
ENST00000684711.1:c.*1856G= ENSP00000506841.1:n.*1856G=
ENST00000302539.9:c.3463G= ENSP00000303960.4:p.Ala1155=
ENST00000389817.8:c.3460G= MANE Select ENSP00000374467.4:p.Ala1154=
ENST00000642271.1:c.3457G= ENSP00000493749.1:p.Ala1153=
ENST00000642579.1:c.1544G=
ENST00000642611.1:n.3414G=
ENST00000642902.1:c.3242G=
ENST00000643260.1:c.3460G= ENSP00000494450.1:p.Ala1154=
ENST00000643562.1:c.*1436G= ENSP00000496124.1:n.*1436G=
ENST00000643925.1:c.1584G=
ENST00000644447.1:c.1816G= ENSP00000496282.1:p.Ala606=
ENST00000644484.1:c.*1715G= ENSP00000493558.1:n.*1715G=
ENST00000644675.1:c.*1632G= ENSP00000494567.1:n.*1632G=
ENST00000644757.1:c.*1745G= ENSP00000495085.1:n.*1745G=
ENST00000644772.1:c.3526G= ENSP00000494321.1:p.Ala1176=
ENST00000645004.1:n.599G=
ENST00000645076.1:c.2659G=
ENST00000645417.1:c.626G=
ENST00000645744.1:c.*1724G= ENSP00000494564.1:n.*1724G=
ENST00000645760.1:c.3735G=
ENST00000645884.1:c.*597G= ENSP00000495516.1:n.*597G=
ENST00000646003.1:c.*1416G= ENSP00000495259.1:n.*1416G=
ENST00000646207.1:c.*1927G= ENSP00000495025.1:n.*1927G=
ENST00000646276.1:c.*1733G= ENSP00000496070.1:n.*1733G=
ENST00000646592.1:c.2766G=
ENST00000646902.1:c.3457G= ENSP00000494101.1:p.Ala1153=
ENST00000646993.1:c.*1856G= ENSP00000493720.1:n.*1856G=
ENST00000647013.1:c.3466G= ENSP00000496741.1:n.3466G=
ENST00000647015.1:c.3211G= ENSP00000495389.1:p.Ala1071=
ENST00000647086.1:c.*3190G= ENSP00000493677.1:n.*3190G=
ENST00000647158.1:c.*1601G= ENSP00000495744.1:n.*1601G=
ENST00000302539.8:c.3463G= ENSP00000303960.4:p.Ala1155=
ENST00000389817.7:c.3460G= ENSP00000374467.3:p.Ala1154=
ENST00000524561.1:n.592G=
ENST00000527905.5:c.*336G= ENSP00000431653.1:n.*336G=
NM_000352.4:c.3460G= NP_000343.2:p.Ala1154=
NM_001287174.1:c.3463G= NP_001274103.1:p.Ala1155=
XM_011520331.1:c.3460G= XP_011518633.1:p.Ala1154=
XM_011520332.1:c.3463G= XP_011518634.1:p.Ala1155=
XM_011520333.1:c.1960G= XP_011518635.1:p.Ala654=
XR_930890.1:n.3526G=
XR_930892.1:n.3426G=
XR_930893.1:n.3423G=
NM_001351295.1:c.3526G= NP_001338224.1:p.Ala1176=
NM_001351296.1:c.3460G= NP_001338225.1:p.Ala1154=
NM_001351297.1:c.3457G= NP_001338226.1:p.Ala1153=
NR_147094.1:n.3609G=
XM_017018197.2:c.3529G= XP_016873686.1:p.Ala1177=
XM_017018199.1:c.3526G= XP_016873688.1:p.Ala1176=
XM_017018201.2:c.3529G= XP_016873690.1:p.Ala1177=
XM_017018202.1:c.2026G= XP_016873691.1:p.Ala676=
XM_017018204.1:c.1417G= XP_016873693.1:p.Ala473=
XM_024448668.1:c.1828G= XP_024304436.1:p.Ala610=
XR_001747945.2:n.3601G=
XR_001747946.2:n.3532G=
XR_002957189.1:n.3681G=
NM_000352.6:c.3460G= MANE Select NP_000343.2:p.Ala1154=
NM_001287174.2:c.3463G= NP_001274103.1:p.Ala1155=
NM_001351295.2:c.3526G= NP_001338224.1:p.Ala1176=
NM_001351296.2:c.3460G= NP_001338225.1:p.Ala1154=
NM_001351297.2:c.3457G= NP_001338226.1:p.Ala1153=
NR_147094.2:n.3609G=
NM_001287174.3:c.3463G= NP_001274103.1:p.Ala1155=