Canonical Allele Identifier: CA1955131344
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17412743T= , CM000673.2:g.17412743T= GRCh38
NC_000011.9:g.17434290T= , CM000673.1:g.17434290T= GRCh37
NC_000011.8:g.17390866T= NCBI36
NG_008867.1:g.69160A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.2148A=
ENST00000529967.6:n.738A=
ENST00000642611.2:n.2548A=
ENST00000682051.1:n.2495A=
ENST00000682110.1:n.2548A=
ENST00000682140.1:c.2476A= ENSP00000507829.1:p.Ile826=
ENST00000682185.1:n.3784A=
ENST00000682204.1:c.*617A= ENSP00000507094.1:n.*617A=
ENST00000682215.1:n.2545A=
ENST00000682288.1:c.*910A= ENSP00000507506.1:n.*910A=
ENST00000682442.1:n.2669A=
ENST00000682528.1:n.2545A=
ENST00000682673.1:n.2492A=
ENST00000682805.1:n.2545A=
ENST00000682965.1:c.2476A= ENSP00000508229.1:p.Ile826=
ENST00000683093.1:n.2647A=
ENST00000683136.1:c.2476A= ENSP00000507768.1:p.Ile826=
ENST00000683153.1:n.2704A=
ENST00000683365.1:n.2650A=
ENST00000683377.1:n.2548A=
ENST00000683456.1:c.2479A= ENSP00000508318.1:p.Ile827=
ENST00000683522.1:n.2548A=
ENST00000683562.1:c.*648A= ENSP00000508265.1:n.*648A=
ENST00000683693.1:n.2545A=
ENST00000683725.1:c.2479A= ENSP00000507496.1:p.Ile827=
ENST00000684010.1:n.2463A=
ENST00000684157.1:n.2548A=
ENST00000684253.1:n.2451A=
ENST00000684288.1:c.*651A= ENSP00000507143.1:n.*651A=
ENST00000684313.1:n.1980A=
ENST00000684332.1:n.2621A=
ENST00000684371.1:n.2654A=
ENST00000684404.1:n.2545A=
ENST00000684442.1:n.2548A=
ENST00000684555.1:c.*691A= ENSP00000507705.1:n.*691A=
ENST00000684571.1:c.2320A= ENSP00000506935.1:p.Ile774=
ENST00000684593.1:c.*2184A= ENSP00000507005.1:n.*2184A=
ENST00000684711.1:c.*875A= ENSP00000506841.1:n.*875A=
ENST00000302539.9:c.2482A= ENSP00000303960.4:p.Ile828=
ENST00000389817.8:c.2479A= MANE Select ENSP00000374467.4:p.Ile827=
ENST00000642271.1:c.2476A= ENSP00000493749.1:p.Ile826=
ENST00000642579.1:c.563A=
ENST00000642611.1:n.2433A=
ENST00000642902.1:c.2314A=
ENST00000643260.1:c.2479A= ENSP00000494450.1:p.Ile827=
ENST00000643562.1:c.*455A= ENSP00000496124.1:n.*455A=
ENST00000643925.1:c.523A=
ENST00000644447.1:c.835A= ENSP00000496282.1:p.Ile279=
ENST00000644472.1:c.*840A= ENSP00000495378.1:n.*840A=
ENST00000644484.1:c.*688A= ENSP00000493558.1:n.*688A=
ENST00000644542.1:c.*2184A= ENSP00000495532.1:n.*2184A=
ENST00000644675.1:c.*651A= ENSP00000494567.1:n.*651A=
ENST00000644757.1:c.*784A= ENSP00000495085.1:n.*784A=
ENST00000644772.1:c.2545A= ENSP00000494321.1:p.Ile849=
ENST00000645076.1:c.1731A=
ENST00000645744.1:c.*843A= ENSP00000494564.1:n.*843A=
ENST00000645760.1:c.2754A=
ENST00000645884.1:c.2479A= ENSP00000495516.1:p.Ile827=
ENST00000646003.1:c.*535A= ENSP00000495259.1:n.*535A=
ENST00000646207.1:c.*843A= ENSP00000495025.1:n.*843A=
ENST00000646276.1:c.*752A= ENSP00000496070.1:n.*752A=
ENST00000646592.1:c.1705A=
ENST00000646902.1:c.2476A= ENSP00000494101.1:p.Ile826=
ENST00000646993.1:c.*875A= ENSP00000493720.1:n.*875A=
ENST00000647013.1:c.2485A= ENSP00000496741.1:n.2485A=
ENST00000647015.1:c.2230A= ENSP00000495389.1:p.Ile744=
ENST00000647086.1:c.*2209A= ENSP00000493677.1:n.*2209A=
ENST00000647158.1:c.*620A= ENSP00000495744.1:n.*620A=
ENST00000302539.8:c.2482A= ENSP00000303960.4:p.Ile828=
ENST00000389817.7:c.2479A= ENSP00000374467.3:p.Ile827=
ENST00000526921.5:n.163A=
ENST00000527905.5:c.2449A= ENSP00000431653.1:p.Ile817=
ENST00000529967.5:n.148A=
ENST00000530147.5:n.62A=
ENST00000531911.1:n.593A=
NM_000352.4:c.2479A= NP_000343.2:p.Ile827=
NM_001287174.1:c.2482A= NP_001274103.1:p.Ile828=
XM_011520331.1:c.2479A= XP_011518633.1:p.Ile827=
XM_011520332.1:c.2482A= XP_011518634.1:p.Ile828=
XM_011520333.1:c.979A= XP_011518635.1:p.Ile327=
XM_011520334.1:c.2482A= XP_011518636.1:p.Ile828=
XR_930890.1:n.2545A=
XR_930891.1:n.2545A=
XR_930892.1:n.2545A=
XR_930893.1:n.2542A=
NM_001351295.1:c.2545A= NP_001338224.1:p.Ile849=
NM_001351296.1:c.2479A= NP_001338225.1:p.Ile827=
NM_001351297.1:c.2476A= NP_001338226.1:p.Ile826=
NR_147094.1:n.2548A=
XM_017018197.2:c.2548A= XP_016873686.1:p.Ile850=
XM_017018199.1:c.2545A= XP_016873688.1:p.Ile849=
XM_017018201.2:c.2548A= XP_016873690.1:p.Ile850=
XM_017018202.1:c.1045A= XP_016873691.1:p.Ile349=
XM_017018204.1:c.436A= XP_016873693.1:p.Ile146=
XM_024448668.1:c.847A= XP_024304436.1:p.Ile283=
XR_001747945.2:n.2620A=
XR_001747946.2:n.2551A=
XR_002957189.1:n.2620A=
NM_000352.6:c.2479A= MANE Select NP_000343.2:p.Ile827=
NM_001287174.2:c.2482A= NP_001274103.1:p.Ile828=
NM_001351295.2:c.2545A= NP_001338224.1:p.Ile849=
NM_001351296.2:c.2479A= NP_001338225.1:p.Ile827=
NM_001351297.2:c.2476A= NP_001338226.1:p.Ile826=
NR_147094.2:n.2548A=
NM_001287174.3:c.2482A= NP_001274103.1:p.Ile828=