Canonical Allele Identifier: CA1955131322
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17412680T= , CM000673.2:g.17412680T= GRCh38
NC_000011.9:g.17434227T= , CM000673.1:g.17434227T= GRCh37
NC_000011.8:g.17390803T= NCBI36
NG_008867.1:g.69223A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.2211A=
ENST00000529967.6:n.801A=
ENST00000642611.2:n.2611A=
ENST00000682051.1:n.2558A=
ENST00000682110.1:n.2611A=
ENST00000682140.1:c.2539A= ENSP00000507829.1:p.Asn847=
ENST00000682185.1:n.3847A=
ENST00000682204.1:c.*680A= ENSP00000507094.1:n.*680A=
ENST00000682215.1:n.2608A=
ENST00000682288.1:c.*973A= ENSP00000507506.1:n.*973A=
ENST00000682442.1:n.2732A=
ENST00000682528.1:n.2608A=
ENST00000682673.1:n.2555A=
ENST00000682805.1:n.2608A=
ENST00000682965.1:c.2539A= ENSP00000508229.1:p.Asn847=
ENST00000683093.1:n.2710A=
ENST00000683136.1:c.2539A= ENSP00000507768.1:p.Asn847=
ENST00000683153.1:n.2767A=
ENST00000683365.1:n.2713A=
ENST00000683377.1:n.2611A=
ENST00000683456.1:c.2542A= ENSP00000508318.1:p.Asn848=
ENST00000683522.1:n.2611A=
ENST00000683562.1:c.*711A= ENSP00000508265.1:n.*711A=
ENST00000683693.1:n.2608A=
ENST00000683725.1:c.2542A= ENSP00000507496.1:p.Asn848=
ENST00000684010.1:n.2526A=
ENST00000684157.1:n.2611A=
ENST00000684253.1:n.2514A=
ENST00000684288.1:c.*714A= ENSP00000507143.1:n.*714A=
ENST00000684313.1:n.2043A=
ENST00000684332.1:n.2684A=
ENST00000684371.1:n.2717A=
ENST00000684404.1:n.2608A=
ENST00000684442.1:n.2611A=
ENST00000684555.1:c.*754A= ENSP00000507705.1:n.*754A=
ENST00000684571.1:c.2383A= ENSP00000506935.1:p.Asn795=
ENST00000684593.1:c.*2247A= ENSP00000507005.1:n.*2247A=
ENST00000684711.1:c.*938A= ENSP00000506841.1:n.*938A=
ENST00000302539.9:c.2545A= ENSP00000303960.4:p.Asn849=
ENST00000389817.8:c.2542A= MANE Select ENSP00000374467.4:p.Asn848=
ENST00000642271.1:c.2539A= ENSP00000493749.1:p.Asn847=
ENST00000642579.1:c.626A=
ENST00000642611.1:n.2496A=
ENST00000642902.1:c.2377A=
ENST00000643260.1:c.2542A= ENSP00000494450.1:p.Asn848=
ENST00000643562.1:c.*518A= ENSP00000496124.1:n.*518A=
ENST00000643925.1:c.586A=
ENST00000644447.1:c.898A= ENSP00000496282.1:p.Asn300=
ENST00000644472.1:c.*903A= ENSP00000495378.1:n.*903A=
ENST00000644484.1:c.*751A= ENSP00000493558.1:n.*751A=
ENST00000644542.1:c.*2247A= ENSP00000495532.1:n.*2247A=
ENST00000644675.1:c.*714A= ENSP00000494567.1:n.*714A=
ENST00000644757.1:c.*847A= ENSP00000495085.1:n.*847A=
ENST00000644772.1:c.2608A= ENSP00000494321.1:p.Asn870=
ENST00000645076.1:c.1794A=
ENST00000645744.1:c.*906A= ENSP00000494564.1:n.*906A=
ENST00000645760.1:c.2817A=
ENST00000645884.1:c.2542A= ENSP00000495516.1:p.Asn848=
ENST00000646003.1:c.*598A= ENSP00000495259.1:n.*598A=
ENST00000646207.1:c.*906A= ENSP00000495025.1:n.*906A=
ENST00000646276.1:c.*815A= ENSP00000496070.1:n.*815A=
ENST00000646592.1:c.1768A=
ENST00000646902.1:c.2539A= ENSP00000494101.1:p.Asn847=
ENST00000646993.1:c.*938A= ENSP00000493720.1:n.*938A=
ENST00000647013.1:c.2548A= ENSP00000496741.1:n.2548A=
ENST00000647015.1:c.2293A= ENSP00000495389.1:p.Asn765=
ENST00000647086.1:c.*2272A= ENSP00000493677.1:n.*2272A=
ENST00000647158.1:c.*683A= ENSP00000495744.1:n.*683A=
ENST00000302539.8:c.2545A= ENSP00000303960.4:p.Asn849=
ENST00000389817.7:c.2542A= ENSP00000374467.3:p.Asn848=
ENST00000526921.5:n.226A=
ENST00000527905.5:c.2512A= ENSP00000431653.1:p.Asn838=
ENST00000529967.5:n.211A=
ENST00000530147.5:n.125A=
ENST00000531911.1:n.656A=
NM_000352.4:c.2542A= NP_000343.2:p.Asn848=
NM_001287174.1:c.2545A= NP_001274103.1:p.Asn849=
XM_011520331.1:c.2542A= XP_011518633.1:p.Asn848=
XM_011520332.1:c.2545A= XP_011518634.1:p.Asn849=
XM_011520333.1:c.1042A= XP_011518635.1:p.Asn348=
XM_011520334.1:c.2545A= XP_011518636.1:p.Asn849=
XR_930890.1:n.2608A=
XR_930891.1:n.2608A=
XR_930892.1:n.2608A=
XR_930893.1:n.2605A=
NM_001351295.1:c.2608A= NP_001338224.1:p.Asn870=
NM_001351296.1:c.2542A= NP_001338225.1:p.Asn848=
NM_001351297.1:c.2539A= NP_001338226.1:p.Asn847=
NR_147094.1:n.2611A=
XM_017018197.2:c.2611A= XP_016873686.1:p.Asn871=
XM_017018199.1:c.2608A= XP_016873688.1:p.Asn870=
XM_017018201.2:c.2611A= XP_016873690.1:p.Asn871=
XM_017018202.1:c.1108A= XP_016873691.1:p.Asn370=
XM_017018204.1:c.499A= XP_016873693.1:p.Asn167=
XM_024448668.1:c.910A= XP_024304436.1:p.Asn304=
XR_001747945.2:n.2683A=
XR_001747946.2:n.2614A=
XR_002957189.1:n.2683A=
NM_000352.6:c.2542A= MANE Select NP_000343.2:p.Asn848=
NM_001287174.2:c.2545A= NP_001274103.1:p.Asn849=
NM_001351295.2:c.2608A= NP_001338224.1:p.Asn870=
NM_001351296.2:c.2542A= NP_001338225.1:p.Asn848=
NM_001351297.2:c.2539A= NP_001338226.1:p.Asn847=
NR_147094.2:n.2611A=
NM_001287174.3:c.2545A= NP_001274103.1:p.Asn849=