Canonical Allele Identifier: CA1955123225
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17395633G= , CM000673.2:g.17395633G= GRCh38
NC_000011.9:g.17417180G= , CM000673.1:g.17417180G= GRCh37
NC_000011.8:g.17373756G= NCBI36
NG_008867.1:g.86270C=

Transcript Alleles

HGVS Amino-acid change
ENST00000524561.2:n.3885C=
ENST00000528374.2:c.875C=
ENST00000529967.6:n.2623C=
ENST00000532220.2:n.3517C=
ENST00000642611.2:n.5617C=
ENST00000644057.2:n.860C=
ENST00000645004.2:n.1783C=
ENST00000682051.1:n.4446C=
ENST00000682110.1:n.4499C=
ENST00000682140.1:c.*70C= ENSP00000507829.1:n.*70C=
ENST00000682185.1:n.5589C=
ENST00000682204.1:c.*2422C= ENSP00000507094.1:n.*2422C=
ENST00000682215.1:n.4866C=
ENST00000682288.1:c.*2715C= ENSP00000507506.1:n.*2715C=
ENST00000682442.1:n.4719C=
ENST00000682528.1:n.4576C=
ENST00000682673.1:n.4443C=
ENST00000682805.1:n.4904C=
ENST00000682965.1:c.*706C= ENSP00000508229.1:n.*706C=
ENST00000683093.1:n.5583C=
ENST00000683136.1:c.4167C= ENSP00000507768.1:p.Pro1389=
ENST00000683153.1:n.4541C=
ENST00000683365.1:n.4601C=
ENST00000683377.1:n.4499C=
ENST00000683456.1:c.*1421C= ENSP00000508318.1:n.*1421C=
ENST00000683522.1:n.4499C=
ENST00000683562.1:c.*2453C= ENSP00000508265.1:n.*2453C=
ENST00000683693.1:n.6064C=
ENST00000683725.1:c.4284C= ENSP00000507496.1:p.Pro1428=
ENST00000684010.1:n.4494C=
ENST00000684157.1:n.5484C=
ENST00000684253.1:n.4402C=
ENST00000684288.1:c.*2456C= ENSP00000507143.1:n.*2456C=
ENST00000684313.1:n.3931C=
ENST00000684332.1:n.4572C=
ENST00000684371.1:n.4605C=
ENST00000684404.1:n.5527C=
ENST00000684442.1:n.4723C=
ENST00000684555.1:c.*2496C= ENSP00000507705.1:n.*2496C=
ENST00000684571.1:c.4125C= ENSP00000506935.1:p.Pro1375=
ENST00000684593.1:c.*3989C= ENSP00000507005.1:n.*3989C=
ENST00000684711.1:c.*2680C= ENSP00000506841.1:n.*2680C=
ENST00000302539.9:c.4287C= ENSP00000303960.4:p.Pro1429=
ENST00000389817.8:c.4284C= MANE Select ENSP00000374467.4:p.Pro1428=
ENST00000642271.1:c.4281C= ENSP00000493749.1:p.Pro1427=
ENST00000642579.1:c.2338C=
ENST00000642611.1:n.5502C=
ENST00000642902.1:c.4066C=
ENST00000643260.1:c.4284C= ENSP00000494450.1:p.Pro1428=
ENST00000643562.1:c.*2406C= ENSP00000496124.1:n.*2406C=
ENST00000643925.1:c.2924C=
ENST00000644057.1:n.361C=
ENST00000644484.1:c.*3670C= ENSP00000493558.1:n.*3670C=
ENST00000644675.1:c.*2456C= ENSP00000494567.1:n.*2456C=
ENST00000644757.1:c.*3202+631C= ENSP00000495085.1:n.*3202+631C=
ENST00000644772.1:c.4350C= ENSP00000494321.1:p.Pro1450=
ENST00000645004.1:n.1977C=
ENST00000645076.1:c.3483C=
ENST00000645417.1:c.1472C=
ENST00000645744.1:c.*3969C= ENSP00000494564.1:n.*3969C=
ENST00000645760.1:c.4705C=
ENST00000645884.1:c.*1567C= ENSP00000495516.1:n.*1567C=
ENST00000646003.1:c.*2306C= ENSP00000495259.1:n.*2306C=
ENST00000646207.1:c.*3121C= ENSP00000495025.1:n.*3121C=
ENST00000646276.1:c.*3688C= ENSP00000496070.1:n.*3688C=
ENST00000646592.1:c.3590C=
ENST00000646902.1:c.4251C= ENSP00000494101.1:p.Pro1417=
ENST00000646993.1:c.*2826C= ENSP00000493720.1:n.*2826C=
ENST00000647013.1:c.4290C= ENSP00000496741.1:n.4290C=
ENST00000647015.1:c.4035C= ENSP00000495389.1:p.Pro1345=
ENST00000647086.1:c.*3870C= ENSP00000493677.1:n.*3870C=
ENST00000647158.1:c.*2571C= ENSP00000495744.1:n.*2571C=
ENST00000302539.8:c.4287C= ENSP00000303960.4:p.Pro1429=
ENST00000389817.7:c.4284C= ENSP00000374467.3:p.Pro1428=
ENST00000525022.1:n.283C=
ENST00000526037.5:n.148C=
ENST00000526168.5:c.72C=
ENST00000531642.5:c.120C=
NM_000352.4:c.4284C= NP_000343.2:p.Pro1428=
NM_001287174.1:c.4287C= NP_001274103.1:p.Pro1429=
XM_011520331.1:c.4284C= XP_011518633.1:p.Pro1428=
XM_011520332.1:c.4287C= XP_011518634.1:p.Pro1429=
XM_011520333.1:c.2784C= XP_011518635.1:p.Pro928=
XR_930890.1:n.4350C=
NM_001351295.1:c.4350C= NP_001338224.1:p.Pro1450=
NM_001351296.1:c.4284C= NP_001338225.1:p.Pro1428=
NM_001351297.1:c.4281C= NP_001338226.1:p.Pro1427=
NR_147094.1:n.4579C=
XM_017018197.2:c.4353C= XP_016873686.1:p.Pro1451=
XM_017018199.1:c.4350C= XP_016873688.1:p.Pro1450=
XM_017018201.2:c.4353C= XP_016873690.1:p.Pro1451=
XM_017018202.1:c.2850C= XP_016873691.1:p.Pro950=
XM_017018204.1:c.2241C= XP_016873693.1:p.Pro747=
XM_024448668.1:c.2652C= XP_024304436.1:p.Pro884=
XR_001747945.2:n.4425C=
XR_001747946.2:n.4356C=
XR_002957189.1:n.6139C=
NM_000352.6:c.4284C= MANE Select NP_000343.2:p.Pro1428=
NM_001287174.2:c.4287C= NP_001274103.1:p.Pro1429=
NM_001351295.2:c.4350C= NP_001338224.1:p.Pro1450=
NM_001351296.2:c.4284C= NP_001338225.1:p.Pro1428=
NM_001351297.2:c.4281C= NP_001338226.1:p.Pro1427=
NR_147094.2:n.4579C=
NM_001287174.3:c.4287C= NP_001274103.1:p.Pro1429=