Canonical Allele Identifier: CA1955129287
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17408461C= , CM000673.2:g.17408461C= GRCh38
NC_000011.9:g.17430008C= , CM000673.1:g.17430008C= GRCh37
NC_000011.8:g.17386584C= NCBI36
NG_008867.1:g.73442G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.2420G=
ENST00000529967.6:n.1010G=
ENST00000532220.2:n.483G=
ENST00000642611.2:n.2820G=
ENST00000682051.1:n.2767G=
ENST00000682110.1:n.2820G=
ENST00000682140.1:c.2748G= ENSP00000507829.1:p.Gln916=
ENST00000682185.1:n.4056G=
ENST00000682204.1:c.*889G= ENSP00000507094.1:n.*889G=
ENST00000682215.1:n.2817G=
ENST00000682288.1:c.*1182G= ENSP00000507506.1:n.*1182G=
ENST00000682442.1:n.2941G=
ENST00000682528.1:n.2817G=
ENST00000682673.1:n.2764G=
ENST00000682805.1:n.2817G=
ENST00000682965.1:c.2748G= ENSP00000508229.1:p.Gln916=
ENST00000683093.1:n.2919G=
ENST00000683136.1:c.2748G= ENSP00000507768.1:p.Gln916=
ENST00000683153.1:n.2976G=
ENST00000683365.1:n.2922G=
ENST00000683377.1:n.2820G=
ENST00000683456.1:c.2751G= ENSP00000508318.1:p.Gln917=
ENST00000683522.1:n.2820G=
ENST00000683562.1:c.*920G= ENSP00000508265.1:n.*920G=
ENST00000683693.1:n.2817G=
ENST00000683725.1:c.2751G= ENSP00000507496.1:p.Gln917=
ENST00000684010.1:n.2735G=
ENST00000684157.1:n.2820G=
ENST00000684253.1:n.2723G=
ENST00000684288.1:c.*923G= ENSP00000507143.1:n.*923G=
ENST00000684313.1:n.2252G=
ENST00000684332.1:n.2893G=
ENST00000684371.1:n.2926G=
ENST00000684404.1:n.2817G=
ENST00000684442.1:n.2820G=
ENST00000684555.1:c.*963G= ENSP00000507705.1:n.*963G=
ENST00000684571.1:c.2592G= ENSP00000506935.1:p.Gln864=
ENST00000684593.1:c.*2456G= ENSP00000507005.1:n.*2456G=
ENST00000684711.1:c.*1147G= ENSP00000506841.1:n.*1147G=
ENST00000302539.9:c.2754G= ENSP00000303960.4:p.Gln918=
ENST00000389817.8:c.2751G= MANE Select ENSP00000374467.4:p.Gln917=
ENST00000642271.1:c.2748G= ENSP00000493749.1:p.Gln916=
ENST00000642579.1:c.835G=
ENST00000642611.1:n.2705G=
ENST00000642902.1:c.2586G=
ENST00000643260.1:c.2751G= ENSP00000494450.1:p.Gln917=
ENST00000643562.1:c.*727G= ENSP00000496124.1:n.*727G=
ENST00000643925.1:c.795G=
ENST00000644447.1:c.1107G= ENSP00000496282.1:p.Gln369=
ENST00000644472.1:c.*1112G= ENSP00000495378.1:n.*1112G=
ENST00000644484.1:c.*960G= ENSP00000493558.1:n.*960G=
ENST00000644542.1:c.*2456G= ENSP00000495532.1:n.*2456G=
ENST00000644675.1:c.*923G= ENSP00000494567.1:n.*923G=
ENST00000644757.1:c.*1056G= ENSP00000495085.1:n.*1056G=
ENST00000644772.1:c.2817G= ENSP00000494321.1:p.Gln939=
ENST00000645076.1:c.2003G=
ENST00000645744.1:c.*1115G= ENSP00000494564.1:n.*1115G=
ENST00000645760.1:c.3026G=
ENST00000645884.1:c.2751G= ENSP00000495516.1:p.Gln917=
ENST00000646003.1:c.*807G= ENSP00000495259.1:n.*807G=
ENST00000646207.1:c.*1115G= ENSP00000495025.1:n.*1115G=
ENST00000646276.1:c.*1024G= ENSP00000496070.1:n.*1024G=
ENST00000646592.1:c.1977G=
ENST00000646902.1:c.2748G= ENSP00000494101.1:p.Gln916=
ENST00000646993.1:c.*1147G= ENSP00000493720.1:n.*1147G=
ENST00000647013.1:c.2757G= ENSP00000496741.1:n.2757G=
ENST00000647015.1:c.2502G= ENSP00000495389.1:p.Gln834=
ENST00000647086.1:c.*2481G= ENSP00000493677.1:n.*2481G=
ENST00000647158.1:c.*892G= ENSP00000495744.1:n.*892G=
ENST00000302539.8:c.2754G= ENSP00000303960.4:p.Gln918=
ENST00000389817.7:c.2751G= ENSP00000374467.3:p.Gln917=
ENST00000526921.5:n.435G=
ENST00000527905.5:c.2721G= ENSP00000431653.1:p.Gln907=
ENST00000529967.5:n.420G=
NM_000352.4:c.2751G= NP_000343.2:p.Gln917=
NM_001287174.1:c.2754G= NP_001274103.1:p.Gln918=
XM_011520331.1:c.2751G= XP_011518633.1:p.Gln917=
XM_011520332.1:c.2754G= XP_011518634.1:p.Gln918=
XM_011520333.1:c.1251G= XP_011518635.1:p.Gln417=
XM_011520334.1:c.2754G= XP_011518636.1:p.Gln918=
XR_930890.1:n.2817G=
XR_930891.1:n.2817G=
XR_930892.1:n.2817G=
XR_930893.1:n.2814G=
NM_001351295.1:c.2817G= NP_001338224.1:p.Gln939=
NM_001351296.1:c.2751G= NP_001338225.1:p.Gln917=
NM_001351297.1:c.2748G= NP_001338226.1:p.Gln916=
NR_147094.1:n.2820G=
XM_017018197.2:c.2820G= XP_016873686.1:p.Gln940=
XM_017018199.1:c.2817G= XP_016873688.1:p.Gln939=
XM_017018201.2:c.2820G= XP_016873690.1:p.Gln940=
XM_017018202.1:c.1317G= XP_016873691.1:p.Gln439=
XM_017018204.1:c.708G= XP_016873693.1:p.Gln236=
XM_024448668.1:c.1119G= XP_024304436.1:p.Gln373=
XR_001747945.2:n.2892G=
XR_001747946.2:n.2823G=
XR_002957189.1:n.2892G=
NM_000352.6:c.2751G= MANE Select NP_000343.2:p.Gln917=
NM_001287174.2:c.2754G= NP_001274103.1:p.Gln918=
NM_001351295.2:c.2817G= NP_001338224.1:p.Gln939=
NM_001351296.2:c.2751G= NP_001338225.1:p.Gln917=
NM_001351297.2:c.2748G= NP_001338226.1:p.Gln916=
NR_147094.2:n.2820G=
NM_001287174.3:c.2754G= NP_001274103.1:p.Gln918=