Canonical Allele Identifier: CA1955127621
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17404638C= , CM000673.2:g.17404638C= GRCh38
NC_000011.9:g.17426185C= , CM000673.1:g.17426185C= GRCh37
NC_000011.8:g.17382761C= NCBI36
NG_008867.1:g.77265G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.3000G=
ENST00000528374.2:c.10G=
ENST00000529967.6:n.1770G=
ENST00000532220.2:n.1163G=
ENST00000642611.2:n.3500G=
ENST00000645004.2:n.930G=
ENST00000682051.1:n.3447G=
ENST00000682110.1:n.3500G=
ENST00000682140.1:c.3428G= ENSP00000507829.1:p.Arg1143=
ENST00000682185.1:n.4736G=
ENST00000682204.1:c.*1569G= ENSP00000507094.1:n.*1569G=
ENST00000682215.1:n.3497G=
ENST00000682288.1:c.*1862G= ENSP00000507506.1:n.*1862G=
ENST00000682442.1:n.3720G=
ENST00000682528.1:n.3577G=
ENST00000682673.1:n.3444G=
ENST00000682805.1:n.3497G=
ENST00000682965.1:c.3396+856G= ENSP00000508229.1:n.3396+856G=
ENST00000683093.1:n.3599G=
ENST00000683136.1:c.3428G= ENSP00000507768.1:p.Arg1143=
ENST00000683153.1:n.3656G=
ENST00000683365.1:n.3602G=
ENST00000683377.1:n.3500G=
ENST00000683456.1:c.*568G= ENSP00000508318.1:n.*568G=
ENST00000683522.1:n.3500G=
ENST00000683562.1:c.*1600G= ENSP00000508265.1:n.*1600G=
ENST00000683693.1:n.3577G=
ENST00000683725.1:c.3431G= ENSP00000507496.1:p.Arg1144=
ENST00000684010.1:n.3495G=
ENST00000684157.1:n.3500G=
ENST00000684253.1:n.3403G=
ENST00000684288.1:c.*1603G= ENSP00000507143.1:n.*1603G=
ENST00000684313.1:n.2932G=
ENST00000684332.1:n.3573G=
ENST00000684371.1:n.3606G=
ENST00000684404.1:n.3543G=
ENST00000684442.1:n.3500G=
ENST00000684555.1:c.*1643G= ENSP00000507705.1:n.*1643G=
ENST00000684571.1:c.3272G= ENSP00000506935.1:p.Arg1091=
ENST00000684593.1:c.*3136G= ENSP00000507005.1:n.*3136G=
ENST00000684711.1:c.*1827G= ENSP00000506841.1:n.*1827G=
ENST00000302539.9:c.3434G= ENSP00000303960.4:p.Arg1145=
ENST00000389817.8:c.3431G= MANE Select ENSP00000374467.4:p.Arg1144=
ENST00000642271.1:c.3428G= ENSP00000493749.1:p.Arg1143=
ENST00000642579.1:c.1515G=
ENST00000642611.1:n.3385G=
ENST00000642902.1:c.3213G=
ENST00000643260.1:c.3431G= ENSP00000494450.1:p.Arg1144=
ENST00000643562.1:c.*1407G= ENSP00000496124.1:n.*1407G=
ENST00000643925.1:c.1555G=
ENST00000644447.1:c.1787G= ENSP00000496282.1:p.Arg596=
ENST00000644484.1:c.*1686G= ENSP00000493558.1:n.*1686G=
ENST00000644675.1:c.*1603G= ENSP00000494567.1:n.*1603G=
ENST00000644757.1:c.*1716G= ENSP00000495085.1:n.*1716G=
ENST00000644772.1:c.3497G= ENSP00000494321.1:p.Arg1166=
ENST00000645004.1:n.570G=
ENST00000645076.1:c.2630G=
ENST00000645417.1:c.597G=
ENST00000645744.1:c.*1695G= ENSP00000494564.1:n.*1695G=
ENST00000645760.1:c.3706G=
ENST00000645884.1:c.*568G= ENSP00000495516.1:n.*568G=
ENST00000646003.1:c.*1387G= ENSP00000495259.1:n.*1387G=
ENST00000646207.1:c.*1898G= ENSP00000495025.1:n.*1898G=
ENST00000646276.1:c.*1704G= ENSP00000496070.1:n.*1704G=
ENST00000646592.1:c.2737G=
ENST00000646902.1:c.3428G= ENSP00000494101.1:p.Arg1143=
ENST00000646993.1:c.*1827G= ENSP00000493720.1:n.*1827G=
ENST00000647013.1:c.3437G= ENSP00000496741.1:n.3437G=
ENST00000647015.1:c.3182G= ENSP00000495389.1:p.Arg1061=
ENST00000647086.1:c.*3161G= ENSP00000493677.1:n.*3161G=
ENST00000647158.1:c.*1572G= ENSP00000495744.1:n.*1572G=
ENST00000302539.8:c.3434G= ENSP00000303960.4:p.Arg1145=
ENST00000389817.7:c.3431G= ENSP00000374467.3:p.Arg1144=
ENST00000524561.1:n.563G=
ENST00000527905.5:c.*307G= ENSP00000431653.1:n.*307G=
NM_000352.4:c.3431G= NP_000343.2:p.Arg1144=
NM_001287174.1:c.3434G= NP_001274103.1:p.Arg1145=
XM_011520331.1:c.3431G= XP_011518633.1:p.Arg1144=
XM_011520332.1:c.3434G= XP_011518634.1:p.Arg1145=
XM_011520333.1:c.1931G= XP_011518635.1:p.Arg644=
XR_930890.1:n.3497G=
XR_930892.1:n.3397G=
XR_930893.1:n.3394G=
NM_001351295.1:c.3497G= NP_001338224.1:p.Arg1166=
NM_001351296.1:c.3431G= NP_001338225.1:p.Arg1144=
NM_001351297.1:c.3428G= NP_001338226.1:p.Arg1143=
NR_147094.1:n.3580G=
XM_017018197.2:c.3500G= XP_016873686.1:p.Arg1167=
XM_017018199.1:c.3497G= XP_016873688.1:p.Arg1166=
XM_017018201.2:c.3500G= XP_016873690.1:p.Arg1167=
XM_017018202.1:c.1997G= XP_016873691.1:p.Arg666=
XM_017018204.1:c.1388G= XP_016873693.1:p.Arg463=
XM_024448668.1:c.1799G= XP_024304436.1:p.Arg600=
XR_001747945.2:n.3572G=
XR_001747946.2:n.3503G=
XR_002957189.1:n.3652G=
NM_000352.6:c.3431G= MANE Select NP_000343.2:p.Arg1144=
NM_001287174.2:c.3434G= NP_001274103.1:p.Arg1145=
NM_001351295.2:c.3497G= NP_001338224.1:p.Arg1166=
NM_001351296.2:c.3431G= NP_001338225.1:p.Arg1144=
NM_001351297.2:c.3428G= NP_001338226.1:p.Arg1143=
NR_147094.2:n.3580G=
NM_001287174.3:c.3434G= NP_001274103.1:p.Arg1145=