Canonical Allele Identifier: CA379805121

Gene: ABCC8

Linked Data

• MyVariant Identifiers: chr11:g.17429988A>C (hg19) ; chr11:g.17408441A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17408441A>C , CM000673.2:g.17408441A>C	GRCh38
NC_000011.9:g.17429988A>C , CM000673.1:g.17429988A>C	GRCh37
NC_000011.8:g.17386564A>C	NCBI36
NG_008867.1:g.73462T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000524561.2:n.2440T>G
ENST00000529967.6:n.1030T>G
ENST00000532220.2:n.503T>G
ENST00000642611.2:n.2840T>G
ENST00000682051.1:n.2787T>G
ENST00000682110.1:n.2840T>G
ENST00000682140.1:c.2768T>G	ENSP00000507829.1:p.Phe923Cys
ENST00000682185.1:n.4076T>G
ENST00000682204.1:c.*909T>G	ENSP00000507094.1:n.*909T>G
ENST00000682215.1:n.2837T>G
ENST00000682288.1:c.*1202T>G	ENSP00000507506.1:n.*1202T>G
ENST00000682442.1:n.2961T>G
ENST00000682528.1:n.2837T>G
ENST00000682673.1:n.2784T>G
ENST00000682805.1:n.2837T>G
ENST00000682965.1:c.2768T>G	ENSP00000508229.1:p.Phe923Cys
ENST00000683093.1:n.2939T>G
ENST00000683136.1:c.2768T>G	ENSP00000507768.1:p.Phe923Cys
ENST00000683153.1:n.2996T>G
ENST00000683365.1:n.2942T>G
ENST00000683377.1:n.2840T>G
ENST00000683456.1:c.2771T>G	ENSP00000508318.1:p.Phe924Cys
ENST00000683522.1:n.2840T>G
ENST00000683562.1:c.*940T>G	ENSP00000508265.1:n.*940T>G
ENST00000683693.1:n.2837T>G
ENST00000683725.1:c.2771T>G	ENSP00000507496.1:p.Phe924Cys
ENST00000684010.1:n.2755T>G
ENST00000684157.1:n.2840T>G
ENST00000684253.1:n.2743T>G
ENST00000684288.1:c.*943T>G	ENSP00000507143.1:n.*943T>G
ENST00000684313.1:n.2272T>G
ENST00000684332.1:n.2913T>G
ENST00000684371.1:n.2946T>G
ENST00000684404.1:n.2837T>G
ENST00000684442.1:n.2840T>G
ENST00000684555.1:c.*983T>G	ENSP00000507705.1:n.*983T>G
ENST00000684571.1:c.2612T>G	ENSP00000506935.1:p.Phe871Cys
ENST00000684593.1:c.*2476T>G	ENSP00000507005.1:n.*2476T>G
ENST00000684711.1:c.*1167T>G	ENSP00000506841.1:n.*1167T>G
ENST00000302539.9:c.2774T>G	ENSP00000303960.4:p.Phe925Cys
ENST00000389817.8:c.2771T>G MANE Select	ENSP00000374467.4:p.Phe924Cys
ENST00000642271.1:c.2768T>G	ENSP00000493749.1:p.Phe923Cys
ENST00000642579.1:c.855T>G
ENST00000642611.1:n.2725T>G
ENST00000642902.1:c.2606T>G
ENST00000643260.1:c.2771T>G	ENSP00000494450.1:p.Phe924Cys
ENST00000643562.1:c.*747T>G	ENSP00000496124.1:n.*747T>G
ENST00000643925.1:c.815T>G
ENST00000644447.1:c.1127T>G	ENSP00000496282.1:p.Phe376Cys
ENST00000644472.1:c.*1132T>G	ENSP00000495378.1:n.*1132T>G
ENST00000644484.1:c.*980T>G	ENSP00000493558.1:n.*980T>G
ENST00000644542.1:c.*2476T>G	ENSP00000495532.1:n.*2476T>G
ENST00000644675.1:c.*943T>G	ENSP00000494567.1:n.*943T>G
ENST00000644757.1:c.*1076T>G	ENSP00000495085.1:n.*1076T>G
ENST00000644772.1:c.2837T>G	ENSP00000494321.1:p.Phe946Cys
ENST00000645076.1:c.2023T>G
ENST00000645744.1:c.*1135T>G	ENSP00000494564.1:n.*1135T>G
ENST00000645760.1:c.3046T>G
ENST00000645884.1:c.2771T>G	ENSP00000495516.1:p.Phe924Cys
ENST00000646003.1:c.*827T>G	ENSP00000495259.1:n.*827T>G
ENST00000646207.1:c.*1135T>G	ENSP00000495025.1:n.*1135T>G
ENST00000646276.1:c.*1044T>G	ENSP00000496070.1:n.*1044T>G
ENST00000646592.1:c.1997T>G
ENST00000646902.1:c.2768T>G	ENSP00000494101.1:p.Phe923Cys
ENST00000646993.1:c.*1167T>G	ENSP00000493720.1:n.*1167T>G
ENST00000647013.1:c.2777T>G	ENSP00000496741.1:n.2777T>G
ENST00000647015.1:c.2522T>G	ENSP00000495389.1:p.Phe841Cys
ENST00000647086.1:c.*2501T>G	ENSP00000493677.1:n.*2501T>G
ENST00000647158.1:c.*912T>G	ENSP00000495744.1:n.*912T>G
ENST00000302539.8:c.2774T>G	ENSP00000303960.4:p.Phe925Cys
ENST00000389817.7:c.2771T>G	ENSP00000374467.3:p.Phe924Cys
ENST00000526921.5:n.455T>G
ENST00000527905.5:c.2741T>G	ENSP00000431653.1:p.Phe914Cys
ENST00000529967.5:n.440T>G
NM_000352.4:c.2771T>G	NP_000343.2:p.Phe924Cys
NM_001287174.1:c.2774T>G	NP_001274103.1:p.Phe925Cys
XM_011520331.1:c.2771T>G	XP_011518633.1:p.Phe924Cys
XM_011520332.1:c.2774T>G	XP_011518634.1:p.Phe925Cys
XM_011520333.1:c.1271T>G	XP_011518635.1:p.Phe424Cys
XM_011520334.1:c.2774T>G	XP_011518636.1:p.Phe925Cys
XR_930890.1:n.2837T>G
XR_930891.1:n.2837T>G
XR_930892.1:n.2837T>G
XR_930893.1:n.2834T>G
NM_001351295.1:c.2837T>G	NP_001338224.1:p.Phe946Cys
NM_001351296.1:c.2771T>G	NP_001338225.1:p.Phe924Cys
NM_001351297.1:c.2768T>G	NP_001338226.1:p.Phe923Cys
NR_147094.1:n.2840T>G
XM_017018197.2:c.2840T>G	XP_016873686.1:p.Phe947Cys
XM_017018199.1:c.2837T>G	XP_016873688.1:p.Phe946Cys
XM_017018201.2:c.2840T>G	XP_016873690.1:p.Phe947Cys
XM_017018202.1:c.1337T>G	XP_016873691.1:p.Phe446Cys
XM_017018204.1:c.728T>G	XP_016873693.1:p.Phe243Cys
XM_024448668.1:c.1139T>G	XP_024304436.1:p.Phe380Cys
XR_001747945.2:n.2912T>G
XR_001747946.2:n.2843T>G
XR_002957189.1:n.2912T>G
NM_000352.6:c.2771T>G MANE Select	NP_000343.2:p.Phe924Cys
NM_001287174.2:c.2774T>G	NP_001274103.1:p.Phe925Cys
NM_001351295.2:c.2837T>G	NP_001338224.1:p.Phe946Cys
NM_001351296.2:c.2771T>G	NP_001338225.1:p.Phe924Cys
NM_001351297.2:c.2768T>G	NP_001338226.1:p.Phe923Cys
NR_147094.2:n.2840T>G
NM_001287174.3:c.2774T>G	NP_001274103.1:p.Phe925Cys