Canonical Allele Identifier: CA473516069
Gene: ABCC8 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.17449860G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17428313G>C , CM000673.2:g.17428313G>C GRCh38
NC_000011.9:g.17449860G>C , CM000673.1:g.17449860G>C GRCh37
NC_000011.8:g.17406436G>C NCBI36
NG_008867.1:g.53590C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.1685C>G
ENST00000529967.6:n.275C>G
ENST00000642611.2:n.2082C>G
ENST00000682051.1:n.2029C>G
ENST00000682110.1:n.2082C>G
ENST00000682140.1:c.2013C>G ENSP00000507829.1:p.Gly671=
ENST00000682185.1:n.3321C>G
ENST00000682204.1:c.*154C>G ENSP00000507094.1:n.*154C>G
ENST00000682215.1:n.2082C>G
ENST00000682288.1:c.*444C>G ENSP00000507506.1:n.*444C>G
ENST00000682442.1:n.2203C>G
ENST00000682528.1:n.2082C>G
ENST00000682673.1:n.2029C>G
ENST00000682805.1:n.2082C>G
ENST00000682965.1:c.2013C>G ENSP00000508229.1:p.Gly671=
ENST00000683093.1:n.2184C>G
ENST00000683136.1:c.2013C>G ENSP00000507768.1:p.Gly671=
ENST00000683153.1:n.2241C>G
ENST00000683253.1:n.3098C>G
ENST00000683365.1:n.2184C>G
ENST00000683377.1:n.2082C>G
ENST00000683456.1:c.2013C>G ENSP00000508318.1:p.Gly671=
ENST00000683522.1:n.2082C>G
ENST00000683562.1:c.*185C>G ENSP00000508265.1:n.*185C>G
ENST00000683693.1:n.2082C>G
ENST00000683725.1:c.2016C>G ENSP00000507496.1:p.Gly672=
ENST00000684010.1:n.2082C>G
ENST00000684157.1:n.2082C>G
ENST00000684253.1:n.1988C>G
ENST00000684288.1:c.*185C>G ENSP00000507143.1:n.*185C>G
ENST00000684313.1:n.1724-11351C>G
ENST00000684332.1:n.2155C>G
ENST00000684371.1:n.2188C>G
ENST00000684404.1:n.2082C>G
ENST00000684442.1:n.2082C>G
ENST00000684555.1:c.*225C>G ENSP00000507705.1:n.*225C>G
ENST00000684571.1:c.1857C>G ENSP00000506935.1:p.Gly619=
ENST00000684593.1:c.*1721C>G ENSP00000507005.1:n.*1721C>G
ENST00000684711.1:c.*412C>G ENSP00000506841.1:n.*412C>G
ENST00000302539.9:c.2016C>G ENSP00000303960.4:p.Gly672=
ENST00000389817.8:c.2016C>G MANE Select ENSP00000374467.4:p.Gly672=
ENST00000532728.6:c.1597C>G
ENST00000642271.1:c.2013C>G ENSP00000493749.1:p.Gly671=
ENST00000642579.1:c.97C>G
ENST00000642611.1:n.1967C>G
ENST00000642902.1:c.1851C>G
ENST00000643260.1:c.2013C>G ENSP00000494450.1:p.Gly671=
ENST00000643562.1:c.2008C>G ENSP00000496124.1:p.Arg670Gly
ENST00000644447.1:c.369C>G ENSP00000496282.1:p.Gly123=
ENST00000644472.1:c.*377C>G ENSP00000495378.1:n.*377C>G
ENST00000644484.1:c.*225C>G ENSP00000493558.1:n.*225C>G
ENST00000644542.1:c.*1718C>G ENSP00000495532.1:n.*1718C>G
ENST00000644649.1:c.1186C>G
ENST00000644675.1:c.*185C>G ENSP00000494567.1:n.*185C>G
ENST00000644757.1:c.*318C>G ENSP00000495085.1:n.*318C>G
ENST00000644772.1:c.2082C>G ENSP00000494321.1:p.Gly694=
ENST00000645076.1:c.1268C>G
ENST00000645744.1:c.*377C>G ENSP00000494564.1:n.*377C>G
ENST00000645760.1:c.2291C>G
ENST00000645884.1:c.2013C>G ENSP00000495516.1:p.Gly671=
ENST00000646003.1:c.*154C>G ENSP00000495259.1:n.*154C>G
ENST00000646207.1:c.*377C>G ENSP00000495025.1:n.*377C>G
ENST00000646276.1:c.*286C>G ENSP00000496070.1:n.*286C>G
ENST00000646592.1:c.1239C>G
ENST00000646902.1:c.2013C>G ENSP00000494101.1:p.Gly671=
ENST00000646993.1:c.*412C>G ENSP00000493720.1:n.*412C>G
ENST00000647013.1:c.2019C>G ENSP00000496741.1:n.2019C>G
ENST00000647015.1:c.1764C>G ENSP00000495389.1:p.Gly588=
ENST00000647086.1:c.*1743C>G ENSP00000493677.1:n.*1743C>G
ENST00000647158.1:c.*154C>G ENSP00000495744.1:n.*154C>G
ENST00000302539.8:c.2016C>G ENSP00000303960.4:p.Gly672=
ENST00000389817.7:c.2016C>G ENSP00000374467.3:p.Gly672=
ENST00000527905.5:c.1986C>G ENSP00000431653.1:p.Gly662=
NM_000352.4:c.2016C>G NP_000343.2:p.Gly672=
NM_001287174.1:c.2016C>G NP_001274103.1:p.Gly672=
XM_011520331.1:c.2013C>G XP_011518633.1:p.Gly671=
XM_011520332.1:c.2016C>G XP_011518634.1:p.Gly672=
XM_011520333.1:c.513C>G XP_011518635.1:p.Gly171=
XM_011520334.1:c.2016C>G XP_011518636.1:p.Gly672=
XR_930890.1:n.2079C>G
XR_930891.1:n.2079C>G
XR_930892.1:n.2079C>G
XR_930893.1:n.2079C>G
NM_001351295.1:c.2082C>G NP_001338224.1:p.Gly694=
NM_001351296.1:c.2013C>G NP_001338225.1:p.Gly671=
NM_001351297.1:c.2013C>G NP_001338226.1:p.Gly671=
NR_147094.1:n.2082C>G
XM_017018197.2:c.2082C>G XP_016873686.1:p.Gly694=
XM_017018199.1:c.2079C>G XP_016873688.1:p.Gly693=
XM_017018201.2:c.2082C>G XP_016873690.1:p.Gly694=
XM_017018202.1:c.579C>G XP_016873691.1:p.Gly193=
XM_017018204.1:c.-28C>G XP_016873693.1:n.-28C>G
XM_024448668.1:c.381C>G XP_024304436.1:p.Gly127=
XR_001747945.2:n.2154C>G
XR_001747946.2:n.2088C>G
XR_002957189.1:n.2154C>G
NM_000352.6:c.2016C>G MANE Select NP_000343.2:p.Gly672=
NM_001287174.2:c.2016C>G NP_001274103.1:p.Gly672=
NM_001351295.2:c.2082C>G NP_001338224.1:p.Gly694=
NM_001351296.2:c.2013C>G NP_001338225.1:p.Gly671=
NM_001351297.2:c.2013C>G NP_001338226.1:p.Gly671=
NR_147094.2:n.2082C>G
NM_001287174.3:c.2016C>G NP_001274103.1:p.Gly672=