Canonical Allele Identifier: CA1955131342
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17412739T= , CM000673.2:g.17412739T= GRCh38
NC_000011.9:g.17434286T= , CM000673.1:g.17434286T= GRCh37
NC_000011.8:g.17390862T= NCBI36
NG_008867.1:g.69164A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.2152A=
ENST00000529967.6:n.742A=
ENST00000642611.2:n.2552A=
ENST00000682051.1:n.2499A=
ENST00000682110.1:n.2552A=
ENST00000682140.1:c.2480A= ENSP00000507829.1:p.Asn827=
ENST00000682185.1:n.3788A=
ENST00000682204.1:c.*621A= ENSP00000507094.1:n.*621A=
ENST00000682215.1:n.2549A=
ENST00000682288.1:c.*914A= ENSP00000507506.1:n.*914A=
ENST00000682442.1:n.2673A=
ENST00000682528.1:n.2549A=
ENST00000682673.1:n.2496A=
ENST00000682805.1:n.2549A=
ENST00000682965.1:c.2480A= ENSP00000508229.1:p.Asn827=
ENST00000683093.1:n.2651A=
ENST00000683136.1:c.2480A= ENSP00000507768.1:p.Asn827=
ENST00000683153.1:n.2708A=
ENST00000683365.1:n.2654A=
ENST00000683377.1:n.2552A=
ENST00000683456.1:c.2483A= ENSP00000508318.1:p.Asn828=
ENST00000683522.1:n.2552A=
ENST00000683562.1:c.*652A= ENSP00000508265.1:n.*652A=
ENST00000683693.1:n.2549A=
ENST00000683725.1:c.2483A= ENSP00000507496.1:p.Asn828=
ENST00000684010.1:n.2467A=
ENST00000684157.1:n.2552A=
ENST00000684253.1:n.2455A=
ENST00000684288.1:c.*655A= ENSP00000507143.1:n.*655A=
ENST00000684313.1:n.1984A=
ENST00000684332.1:n.2625A=
ENST00000684371.1:n.2658A=
ENST00000684404.1:n.2549A=
ENST00000684442.1:n.2552A=
ENST00000684555.1:c.*695A= ENSP00000507705.1:n.*695A=
ENST00000684571.1:c.2324A= ENSP00000506935.1:p.Asn775=
ENST00000684593.1:c.*2188A= ENSP00000507005.1:n.*2188A=
ENST00000684711.1:c.*879A= ENSP00000506841.1:n.*879A=
ENST00000302539.9:c.2486A= ENSP00000303960.4:p.Asn829=
ENST00000389817.8:c.2483A= MANE Select ENSP00000374467.4:p.Asn828=
ENST00000642271.1:c.2480A= ENSP00000493749.1:p.Asn827=
ENST00000642579.1:c.567A=
ENST00000642611.1:n.2437A=
ENST00000642902.1:c.2318A=
ENST00000643260.1:c.2483A= ENSP00000494450.1:p.Asn828=
ENST00000643562.1:c.*459A= ENSP00000496124.1:n.*459A=
ENST00000643925.1:c.527A=
ENST00000644447.1:c.839A= ENSP00000496282.1:p.Asn280=
ENST00000644472.1:c.*844A= ENSP00000495378.1:n.*844A=
ENST00000644484.1:c.*692A= ENSP00000493558.1:n.*692A=
ENST00000644542.1:c.*2188A= ENSP00000495532.1:n.*2188A=
ENST00000644675.1:c.*655A= ENSP00000494567.1:n.*655A=
ENST00000644757.1:c.*788A= ENSP00000495085.1:n.*788A=
ENST00000644772.1:c.2549A= ENSP00000494321.1:p.Asn850=
ENST00000645076.1:c.1735A=
ENST00000645744.1:c.*847A= ENSP00000494564.1:n.*847A=
ENST00000645760.1:c.2758A=
ENST00000645884.1:c.2483A= ENSP00000495516.1:p.Asn828=
ENST00000646003.1:c.*539A= ENSP00000495259.1:n.*539A=
ENST00000646207.1:c.*847A= ENSP00000495025.1:n.*847A=
ENST00000646276.1:c.*756A= ENSP00000496070.1:n.*756A=
ENST00000646592.1:c.1709A=
ENST00000646902.1:c.2480A= ENSP00000494101.1:p.Asn827=
ENST00000646993.1:c.*879A= ENSP00000493720.1:n.*879A=
ENST00000647013.1:c.2489A= ENSP00000496741.1:n.2489A=
ENST00000647015.1:c.2234A= ENSP00000495389.1:p.Asn745=
ENST00000647086.1:c.*2213A= ENSP00000493677.1:n.*2213A=
ENST00000647158.1:c.*624A= ENSP00000495744.1:n.*624A=
ENST00000302539.8:c.2486A= ENSP00000303960.4:p.Asn829=
ENST00000389817.7:c.2483A= ENSP00000374467.3:p.Asn828=
ENST00000526921.5:n.167A=
ENST00000527905.5:c.2453A= ENSP00000431653.1:p.Asn818=
ENST00000529967.5:n.152A=
ENST00000530147.5:n.66A=
ENST00000531911.1:n.597A=
NM_000352.4:c.2483A= NP_000343.2:p.Asn828=
NM_001287174.1:c.2486A= NP_001274103.1:p.Asn829=
XM_011520331.1:c.2483A= XP_011518633.1:p.Asn828=
XM_011520332.1:c.2486A= XP_011518634.1:p.Asn829=
XM_011520333.1:c.983A= XP_011518635.1:p.Asn328=
XM_011520334.1:c.2486A= XP_011518636.1:p.Asn829=
XR_930890.1:n.2549A=
XR_930891.1:n.2549A=
XR_930892.1:n.2549A=
XR_930893.1:n.2546A=
NM_001351295.1:c.2549A= NP_001338224.1:p.Asn850=
NM_001351296.1:c.2483A= NP_001338225.1:p.Asn828=
NM_001351297.1:c.2480A= NP_001338226.1:p.Asn827=
NR_147094.1:n.2552A=
XM_017018197.2:c.2552A= XP_016873686.1:p.Asn851=
XM_017018199.1:c.2549A= XP_016873688.1:p.Asn850=
XM_017018201.2:c.2552A= XP_016873690.1:p.Asn851=
XM_017018202.1:c.1049A= XP_016873691.1:p.Asn350=
XM_017018204.1:c.440A= XP_016873693.1:p.Asn147=
XM_024448668.1:c.851A= XP_024304436.1:p.Asn284=
XR_001747945.2:n.2624A=
XR_001747946.2:n.2555A=
XR_002957189.1:n.2624A=
NM_000352.6:c.2483A= MANE Select NP_000343.2:p.Asn828=
NM_001287174.2:c.2486A= NP_001274103.1:p.Asn829=
NM_001351295.2:c.2549A= NP_001338224.1:p.Asn850=
NM_001351296.2:c.2483A= NP_001338225.1:p.Asn828=
NM_001351297.2:c.2480A= NP_001338226.1:p.Asn827=
NR_147094.2:n.2552A=
NM_001287174.3:c.2486A= NP_001274103.1:p.Asn829=