Canonical Allele Identifier: CA3435237

Gene: STING1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139476325T>C , CM000667.2:g.139476325T>C	GRCh38
NC_000005.9:g.138855910T>C , CM000667.1:g.138855910T>C	GRCh37
NC_000005.8:g.138836094T>C	NCBI36
NG_034249.1:g.11466A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_198282.4:c.1076A>G MANE Select	NP_938023.1:p.Gln359Arg
ENST00000330794.9:c.1076A>G MANE Select	ENSP00000331288.4:p.Gln359Arg
NM_001301738.1:c.*37A>G	NP_001288667.1:n.*37A>G
NM_001301738.2:c.*37A>G	NP_001288667.1:n.*37A>G
NM_001367258.1:c.719A>G	NP_001354187.1:p.Gln240Arg
NM_198282.3:c.1076A>G	NP_938023.1:p.Gln359Arg
ENST00000330794.8:c.1076A>G	ENSP00000331288.4:p.Gln359Arg
ENST00000502362.2:n.1851A>G
ENST00000507297.5:n.2409A>G
ENST00000509573.5:n.688A>G
ENST00000511886.6:n.2182A>G
ENST00000512606.5:n.814A>G
ENST00000512606.6:n.1312A>G
ENST00000514119.6:n.1108A>G
ENST00000650883.1:c.*493A>G	ENSP00000499142.1:n.*493A>G
ENST00000651565.1:c.719A>G	ENSP00000498768.1:p.Gln240Arg
ENST00000651699.1:c.1076A>G	ENSP00000499166.1:p.Gln359Arg
ENST00000652110.1:c.*37A>G	ENSP00000498513.1:n.*37A>G
ENST00000652271.1:c.1076A>G	ENSP00000498596.1:p.Gln359Arg
ENST00000652293.1:n.1884A>G
ENST00000652543.1:c.*37A>G	ENSP00000498683.1:n.*37A>G
ENST00000652640.1:n.1463A>G
XM_005268445.2:c.*37A>G	XP_005268502.1:n.*37A>G
XM_005268445.4:c.*37A>G	XP_005268502.1:n.*37A>G
XM_011537640.1:c.719A>G	XP_011535942.1:p.Gln240Arg
XM_011537640.2:c.719A>G	XP_011535942.1:p.Gln240Arg