Canonical Allele Identifier: CA1955123337
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17395856G= , CM000673.2:g.17395856G= GRCh38
NC_000011.9:g.17417403G= , CM000673.1:g.17417403G= GRCh37
NC_000011.8:g.17373979G= NCBI36
NG_008867.1:g.86047C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.3795C=
ENST00000528374.2:c.785C=
ENST00000529967.6:n.2533C=
ENST00000532220.2:n.3427C=
ENST00000642611.2:n.5394C=
ENST00000644057.2:n.637C=
ENST00000645004.2:n.1693C=
ENST00000682051.1:n.4356C=
ENST00000682110.1:n.4409C=
ENST00000682140.1:c.4060C= ENSP00000507829.1:p.Arg1354=
ENST00000682185.1:n.5499C=
ENST00000682204.1:c.*2332C= ENSP00000507094.1:n.*2332C=
ENST00000682215.1:n.4776C=
ENST00000682288.1:c.*2625C= ENSP00000507506.1:n.*2625C=
ENST00000682442.1:n.4629C=
ENST00000682528.1:n.4486C=
ENST00000682673.1:n.4353C=
ENST00000682805.1:n.4814C=
ENST00000682965.1:c.*616C= ENSP00000508229.1:n.*616C=
ENST00000683093.1:n.5493C=
ENST00000683136.1:c.4077C= ENSP00000507768.1:p.Phe1359=
ENST00000683153.1:n.4451C=
ENST00000683365.1:n.4511C=
ENST00000683377.1:n.4409C=
ENST00000683456.1:c.*1331C= ENSP00000508318.1:n.*1331C=
ENST00000683522.1:n.4409C=
ENST00000683562.1:c.*2363C= ENSP00000508265.1:n.*2363C=
ENST00000683693.1:n.5841C=
ENST00000683725.1:c.4194C= ENSP00000507496.1:p.Phe1398=
ENST00000684010.1:n.4404C=
ENST00000684157.1:n.5394C=
ENST00000684253.1:n.4312C=
ENST00000684288.1:c.*2366C= ENSP00000507143.1:n.*2366C=
ENST00000684313.1:n.3841C=
ENST00000684332.1:n.4482C=
ENST00000684371.1:n.4515C=
ENST00000684404.1:n.5437C=
ENST00000684442.1:n.4633C=
ENST00000684555.1:c.*2406C= ENSP00000507705.1:n.*2406C=
ENST00000684571.1:c.4035C= ENSP00000506935.1:p.Phe1345=
ENST00000684593.1:c.*3899C= ENSP00000507005.1:n.*3899C=
ENST00000684711.1:c.*2590C= ENSP00000506841.1:n.*2590C=
ENST00000302539.9:c.4197C= ENSP00000303960.4:p.Phe1399=
ENST00000389817.8:c.4194C= MANE Select ENSP00000374467.4:p.Phe1398=
ENST00000642271.1:c.4191C= ENSP00000493749.1:p.Phe1397=
ENST00000642579.1:c.2248C=
ENST00000642611.1:n.5279C=
ENST00000642902.1:c.3976C=
ENST00000643260.1:c.4194C= ENSP00000494450.1:p.Phe1398=
ENST00000643562.1:c.*2316C= ENSP00000496124.1:n.*2316C=
ENST00000643925.1:c.2834C=
ENST00000644057.1:n.271C=
ENST00000644484.1:c.*3580C= ENSP00000493558.1:n.*3580C=
ENST00000644675.1:c.*2366C= ENSP00000494567.1:n.*2366C=
ENST00000644757.1:c.*3202+408C= ENSP00000495085.1:n.*3202+408C=
ENST00000644772.1:c.4260C= ENSP00000494321.1:p.Phe1420=
ENST00000645004.1:n.1887C=
ENST00000645076.1:c.3393C=
ENST00000645417.1:c.1382C=
ENST00000645744.1:c.*3959C= ENSP00000494564.1:n.*3959C=
ENST00000645760.1:c.4615C=
ENST00000645884.1:c.*1477C= ENSP00000495516.1:n.*1477C=
ENST00000646003.1:c.*2296C= ENSP00000495259.1:n.*2296C=
ENST00000646207.1:c.*3031C= ENSP00000495025.1:n.*3031C=
ENST00000646276.1:c.*3598C= ENSP00000496070.1:n.*3598C=
ENST00000646592.1:c.3500C=
ENST00000646902.1:c.4161C= ENSP00000494101.1:p.Phe1387=
ENST00000646993.1:c.*2736C= ENSP00000493720.1:n.*2736C=
ENST00000647013.1:c.4200C= ENSP00000496741.1:n.4200C=
ENST00000647015.1:c.3945C= ENSP00000495389.1:p.Phe1315=
ENST00000647086.1:c.*3780C= ENSP00000493677.1:n.*3780C=
ENST00000647158.1:c.*2481C= ENSP00000495744.1:n.*2481C=
ENST00000302539.8:c.4197C= ENSP00000303960.4:p.Phe1399=
ENST00000389817.7:c.4194C= ENSP00000374467.3:p.Phe1398=
ENST00000525022.1:n.60C=
ENST00000526168.5:c.62C=
ENST00000531642.5:c.30C=
NM_000352.4:c.4194C= NP_000343.2:p.Phe1398=
NM_001287174.1:c.4197C= NP_001274103.1:p.Phe1399=
XM_011520331.1:c.4194C= XP_011518633.1:p.Phe1398=
XM_011520332.1:c.4197C= XP_011518634.1:p.Phe1399=
XM_011520333.1:c.2694C= XP_011518635.1:p.Phe898=
XR_930890.1:n.4260C=
NM_001351295.1:c.4260C= NP_001338224.1:p.Phe1420=
NM_001351296.1:c.4194C= NP_001338225.1:p.Phe1398=
NM_001351297.1:c.4191C= NP_001338226.1:p.Phe1397=
NR_147094.1:n.4489C=
XM_017018197.2:c.4263C= XP_016873686.1:p.Phe1421=
XM_017018199.1:c.4260C= XP_016873688.1:p.Phe1420=
XM_017018201.2:c.4263C= XP_016873690.1:p.Phe1421=
XM_017018202.1:c.2760C= XP_016873691.1:p.Phe920=
XM_017018204.1:c.2151C= XP_016873693.1:p.Phe717=
XM_024448668.1:c.2562C= XP_024304436.1:p.Phe854=
XR_001747945.2:n.4335C=
XR_001747946.2:n.4266C=
XR_002957189.1:n.5916C=
NM_000352.6:c.4194C= MANE Select NP_000343.2:p.Phe1398=
NM_001287174.2:c.4197C= NP_001274103.1:p.Phe1399=
NM_001351295.2:c.4260C= NP_001338224.1:p.Phe1420=
NM_001351296.2:c.4194C= NP_001338225.1:p.Phe1398=
NM_001351297.2:c.4191C= NP_001338226.1:p.Phe1397=
NR_147094.2:n.4489C=
NM_001287174.3:c.4197C= NP_001274103.1:p.Phe1399=