Canonical Allele Identifier: CA379805204

Gene: ABCC8

Linked Data

• MyVariant Identifiers: chr11:g.17430000T>A (hg19) ; chr11:g.17408453T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17408453T>A , CM000673.2:g.17408453T>A	GRCh38
NC_000011.9:g.17430000T>A , CM000673.1:g.17430000T>A	GRCh37
NC_000011.8:g.17386576T>A	NCBI36
NG_008867.1:g.73450A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524561.2:n.2428A>T
ENST00000529967.6:n.1018A>T
ENST00000532220.2:n.491A>T
ENST00000642611.2:n.2828A>T
ENST00000682051.1:n.2775A>T
ENST00000682110.1:n.2828A>T
ENST00000682140.1:c.2756A>T	ENSP00000507829.1:p.Glu919Val
ENST00000682185.1:n.4064A>T
ENST00000682204.1:c.*897A>T	ENSP00000507094.1:n.*897A>T
ENST00000682215.1:n.2825A>T
ENST00000682288.1:c.*1190A>T	ENSP00000507506.1:n.*1190A>T
ENST00000682442.1:n.2949A>T
ENST00000682528.1:n.2825A>T
ENST00000682673.1:n.2772A>T
ENST00000682805.1:n.2825A>T
ENST00000682965.1:c.2756A>T	ENSP00000508229.1:p.Glu919Val
ENST00000683093.1:n.2927A>T
ENST00000683136.1:c.2756A>T	ENSP00000507768.1:p.Glu919Val
ENST00000683153.1:n.2984A>T
ENST00000683365.1:n.2930A>T
ENST00000683377.1:n.2828A>T
ENST00000683456.1:c.2759A>T	ENSP00000508318.1:p.Glu920Val
ENST00000683522.1:n.2828A>T
ENST00000683562.1:c.*928A>T	ENSP00000508265.1:n.*928A>T
ENST00000683693.1:n.2825A>T
ENST00000683725.1:c.2759A>T	ENSP00000507496.1:p.Glu920Val
ENST00000684010.1:n.2743A>T
ENST00000684157.1:n.2828A>T
ENST00000684253.1:n.2731A>T
ENST00000684288.1:c.*931A>T	ENSP00000507143.1:n.*931A>T
ENST00000684313.1:n.2260A>T
ENST00000684332.1:n.2901A>T
ENST00000684371.1:n.2934A>T
ENST00000684404.1:n.2825A>T
ENST00000684442.1:n.2828A>T
ENST00000684555.1:c.*971A>T	ENSP00000507705.1:n.*971A>T
ENST00000684571.1:c.2600A>T	ENSP00000506935.1:p.Glu867Val
ENST00000684593.1:c.*2464A>T	ENSP00000507005.1:n.*2464A>T
ENST00000684711.1:c.*1155A>T	ENSP00000506841.1:n.*1155A>T
ENST00000302539.9:c.2762A>T	ENSP00000303960.4:p.Glu921Val
ENST00000389817.8:c.2759A>T MANE Select	ENSP00000374467.4:p.Glu920Val
ENST00000642271.1:c.2756A>T	ENSP00000493749.1:p.Glu919Val
ENST00000642579.1:c.843A>T
ENST00000642611.1:n.2713A>T
ENST00000642902.1:c.2594A>T
ENST00000643260.1:c.2759A>T	ENSP00000494450.1:p.Glu920Val
ENST00000643562.1:c.*735A>T	ENSP00000496124.1:n.*735A>T
ENST00000643925.1:c.803A>T
ENST00000644447.1:c.1115A>T	ENSP00000496282.1:p.Glu372Val
ENST00000644472.1:c.*1120A>T	ENSP00000495378.1:n.*1120A>T
ENST00000644484.1:c.*968A>T	ENSP00000493558.1:n.*968A>T
ENST00000644542.1:c.*2464A>T	ENSP00000495532.1:n.*2464A>T
ENST00000644675.1:c.*931A>T	ENSP00000494567.1:n.*931A>T
ENST00000644757.1:c.*1064A>T	ENSP00000495085.1:n.*1064A>T
ENST00000644772.1:c.2825A>T	ENSP00000494321.1:p.Glu942Val
ENST00000645076.1:c.2011A>T
ENST00000645744.1:c.*1123A>T	ENSP00000494564.1:n.*1123A>T
ENST00000645760.1:c.3034A>T
ENST00000645884.1:c.2759A>T	ENSP00000495516.1:p.Glu920Val
ENST00000646003.1:c.*815A>T	ENSP00000495259.1:n.*815A>T
ENST00000646207.1:c.*1123A>T	ENSP00000495025.1:n.*1123A>T
ENST00000646276.1:c.*1032A>T	ENSP00000496070.1:n.*1032A>T
ENST00000646592.1:c.1985A>T
ENST00000646902.1:c.2756A>T	ENSP00000494101.1:p.Glu919Val
ENST00000646993.1:c.*1155A>T	ENSP00000493720.1:n.*1155A>T
ENST00000647013.1:c.2765A>T	ENSP00000496741.1:n.2765A>T
ENST00000647015.1:c.2510A>T	ENSP00000495389.1:p.Glu837Val
ENST00000647086.1:c.*2489A>T	ENSP00000493677.1:n.*2489A>T
ENST00000647158.1:c.*900A>T	ENSP00000495744.1:n.*900A>T
ENST00000302539.8:c.2762A>T	ENSP00000303960.4:p.Glu921Val
ENST00000389817.7:c.2759A>T	ENSP00000374467.3:p.Glu920Val
ENST00000526921.5:n.443A>T
ENST00000527905.5:c.2729A>T	ENSP00000431653.1:p.Glu910Val
ENST00000529967.5:n.428A>T
NM_000352.4:c.2759A>T	NP_000343.2:p.Glu920Val
NM_001287174.1:c.2762A>T	NP_001274103.1:p.Glu921Val
XM_011520331.1:c.2759A>T	XP_011518633.1:p.Glu920Val
XM_011520332.1:c.2762A>T	XP_011518634.1:p.Glu921Val
XM_011520333.1:c.1259A>T	XP_011518635.1:p.Glu420Val
XM_011520334.1:c.2762A>T	XP_011518636.1:p.Glu921Val
XR_930890.1:n.2825A>T
XR_930891.1:n.2825A>T
XR_930892.1:n.2825A>T
XR_930893.1:n.2822A>T
NM_001351295.1:c.2825A>T	NP_001338224.1:p.Glu942Val
NM_001351296.1:c.2759A>T	NP_001338225.1:p.Glu920Val
NM_001351297.1:c.2756A>T	NP_001338226.1:p.Glu919Val
NR_147094.1:n.2828A>T
XM_017018197.2:c.2828A>T	XP_016873686.1:p.Glu943Val
XM_017018199.1:c.2825A>T	XP_016873688.1:p.Glu942Val
XM_017018201.2:c.2828A>T	XP_016873690.1:p.Glu943Val
XM_017018202.1:c.1325A>T	XP_016873691.1:p.Glu442Val
XM_017018204.1:c.716A>T	XP_016873693.1:p.Glu239Val
XM_024448668.1:c.1127A>T	XP_024304436.1:p.Glu376Val
XR_001747945.2:n.2900A>T
XR_001747946.2:n.2831A>T
XR_002957189.1:n.2900A>T
NM_000352.6:c.2759A>T MANE Select	NP_000343.2:p.Glu920Val
NM_001287174.2:c.2762A>T	NP_001274103.1:p.Glu921Val
NM_001351295.2:c.2825A>T	NP_001338224.1:p.Glu942Val
NM_001351296.2:c.2759A>T	NP_001338225.1:p.Glu920Val
NM_001351297.2:c.2756A>T	NP_001338226.1:p.Glu919Val
NR_147094.2:n.2828A>T
NM_001287174.3:c.2762A>T	NP_001274103.1:p.Glu921Val