Canonical Allele Identifier: CA1955123995
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17397125C= , CM000673.2:g.17397125C= GRCh38
NC_000011.9:g.17418672C= , CM000673.1:g.17418672C= GRCh37
NC_000011.8:g.17375248C= NCBI36
NG_008867.1:g.84778G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.3511G=
ENST00000528374.2:c.568-67G=
ENST00000529967.6:n.2327+68G=
ENST00000532220.2:n.2158G=
ENST00000642611.2:n.4125G=
ENST00000644057.2:n.431+68G=
ENST00000645004.2:n.1487+68G=
ENST00000682051.1:n.4072G=
ENST00000682110.1:n.4125G=
ENST00000682140.1:c.3985+68G= ENSP00000507829.1:n.3985+68G=
ENST00000682185.1:n.5293+68G=
ENST00000682204.1:c.*2126+68G= ENSP00000507094.1:n.*2126+68G=
ENST00000682215.1:n.4492G=
ENST00000682288.1:c.*2419+68G= ENSP00000507506.1:n.*2419+68G=
ENST00000682442.1:n.4345G=
ENST00000682528.1:n.4202G=
ENST00000682673.1:n.4069G=
ENST00000682805.1:n.4492G=
ENST00000682965.1:c.*410+68G= ENSP00000508229.1:n.*410+68G=
ENST00000683093.1:n.4224G=
ENST00000683136.1:c.3871+68G= ENSP00000507768.1:n.3871+68G=
ENST00000683153.1:n.4167G=
ENST00000683365.1:n.4227G=
ENST00000683377.1:n.4125G=
ENST00000683456.1:c.*1125+68G= ENSP00000508318.1:n.*1125+68G=
ENST00000683522.1:n.4125G=
ENST00000683562.1:c.*2157+68G= ENSP00000508265.1:n.*2157+68G=
ENST00000683693.1:n.4572G=
ENST00000683725.1:c.3988+68G= ENSP00000507496.1:n.3988+68G=
ENST00000684010.1:n.4120G=
ENST00000684157.1:n.4125G=
ENST00000684253.1:n.4028G=
ENST00000684288.1:c.*2160+68G= ENSP00000507143.1:n.*2160+68G=
ENST00000684313.1:n.3557G=
ENST00000684332.1:n.4198G=
ENST00000684371.1:n.4231G=
ENST00000684404.1:n.4168G=
ENST00000684442.1:n.4427+68G=
ENST00000684555.1:c.*2200+68G= ENSP00000507705.1:n.*2200+68G=
ENST00000684571.1:c.3829+68G= ENSP00000506935.1:n.3829+68G=
ENST00000684593.1:c.*3693+68G= ENSP00000507005.1:n.*3693+68G=
ENST00000684711.1:c.*2384+68G= ENSP00000506841.1:n.*2384+68G=
ENST00000302539.9:c.3991+68G= ENSP00000303960.4:n.3991+68G=
ENST00000389817.8:c.3988+68G= MANE Select ENSP00000374467.4:n.3988+68G=
ENST00000642271.1:c.3985+68G= ENSP00000493749.1:n.3985+68G=
ENST00000642579.1:c.2072+68G=
ENST00000642611.1:n.4010G=
ENST00000642902.1:c.3770+68G=
ENST00000643260.1:c.3988+68G= ENSP00000494450.1:n.3988+68G=
ENST00000643562.1:c.*2032G= ENSP00000496124.1:n.*2032G=
ENST00000643925.1:c.2550G=
ENST00000644484.1:c.*2311G= ENSP00000493558.1:n.*2311G=
ENST00000644675.1:c.*2160+68G= ENSP00000494567.1:n.*2160+68G=
ENST00000644757.1:c.*2341G= ENSP00000495085.1:n.*2341G=
ENST00000644772.1:c.4054+68G= ENSP00000494321.1:n.4054+68G=
ENST00000645004.1:n.1565G=
ENST00000645076.1:c.3187+68G=
ENST00000645417.1:c.1176+68G=
ENST00000645744.1:c.*2690G= ENSP00000494564.1:n.*2690G=
ENST00000645760.1:c.4331G=
ENST00000645884.1:c.*1193G= ENSP00000495516.1:n.*1193G=
ENST00000646003.1:c.*2012G= ENSP00000495259.1:n.*2012G=
ENST00000646207.1:c.*2825+68G= ENSP00000495025.1:n.*2825+68G=
ENST00000646276.1:c.*2329G= ENSP00000496070.1:n.*2329G=
ENST00000646592.1:c.3294+68G=
ENST00000646902.1:c.3985+68G= ENSP00000494101.1:n.3985+68G=
ENST00000646993.1:c.*2452G= ENSP00000493720.1:n.*2452G=
ENST00000647013.1:c.3994+68G= ENSP00000496741.1:n.3994+68G=
ENST00000647015.1:c.3739+68G= ENSP00000495389.1:n.3739+68G=
ENST00000647086.1:c.*3604+68G= ENSP00000493677.1:n.*3604+68G=
ENST00000647158.1:c.*2197G= ENSP00000495744.1:n.*2197G=
ENST00000302539.8:c.3991+68G= ENSP00000303960.4:n.3991+68G=
ENST00000389817.7:c.3988+68G= ENSP00000374467.3:n.3988+68G=
ENST00000527905.5:c.*932G= ENSP00000431653.1:n.*932G=
ENST00000528374.1:c.459-67G=
ENST00000531137.1:n.475G=
ENST00000531891.1:c.356+68G=
ENST00000532220.1:n.384G=
NM_000352.4:c.3988+68G= NP_000343.2:n.3988+68G=
NM_001287174.1:c.3991+68G= NP_001274103.1:n.3991+68G=
XM_011520331.1:c.3988+68G= XP_011518633.1:n.3988+68G=
XM_011520332.1:c.3991+68G= XP_011518634.1:n.3991+68G=
XM_011520333.1:c.2488+68G= XP_011518635.1:n.2488+68G=
XR_930890.1:n.4054+68G=
NM_001351295.1:c.4054+68G= NP_001338224.1:n.4054+68G=
NM_001351296.1:c.3988+68G= NP_001338225.1:n.3988+68G=
NM_001351297.1:c.3985+68G= NP_001338226.1:n.3985+68G=
NR_147094.1:n.4205G=
XM_017018197.2:c.4057+68G= XP_016873686.1:n.4057+68G=
XM_017018199.1:c.4054+68G= XP_016873688.1:n.4054+68G=
XM_017018201.2:c.4057+68G= XP_016873690.1:n.4057+68G=
XM_017018202.1:c.2554+68G= XP_016873691.1:n.2554+68G=
XM_017018204.1:c.1945+68G= XP_016873693.1:n.1945+68G=
XM_024448668.1:c.2356+68G= XP_024304436.1:n.2356+68G=
XR_001747945.2:n.4129+68G=
XR_001747946.2:n.4060+68G=
XR_002957189.1:n.4647G=
NM_000352.6:c.3988+68G= MANE Select NP_000343.2:n.3988+68G=
NM_001287174.2:c.3991+68G= NP_001274103.1:n.3991+68G=
NM_001351295.2:c.4054+68G= NP_001338224.1:n.4054+68G=
NM_001351296.2:c.3988+68G= NP_001338225.1:n.3988+68G=
NM_001351297.2:c.3985+68G= NP_001338226.1:n.3985+68G=
NR_147094.2:n.4205G=
NM_001287174.3:c.3991+68G= NP_001274103.1:n.3991+68G=