Canonical Allele Identifier: CA361480166

Gene: STING1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139478413A>C , CM000667.2:g.139478413A>C	GRCh38
NC_000005.9:g.138857998A>C , CM000667.1:g.138857998A>C	GRCh37
NC_000005.8:g.138838182A>C	NCBI36
NG_034249.1:g.9378T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_198282.4:c.616T>G MANE Select	NP_938023.1:p.Cys206Gly
ENST00000330794.9:c.616T>G MANE Select	ENSP00000331288.4:p.Cys206Gly
NM_001301738.1:c.616T>G	NP_001288667.1:p.Cys206Gly
NM_001301738.2:c.616T>G	NP_001288667.1:p.Cys206Gly
NM_001367258.1:c.259T>G	NP_001354187.1:p.Cys87Gly
NM_198282.3:c.616T>G	NP_938023.1:p.Cys206Gly
ENST00000330794.8:c.616T>G	ENSP00000331288.4:p.Cys206Gly
ENST00000502362.2:n.1391T>G
ENST00000502825.1:n.394T>G
ENST00000503287.5:n.508T>G
ENST00000507297.5:n.1949T>G
ENST00000509573.5:n.415T>G
ENST00000510817.1:c.616T>G	ENSP00000427455.1:p.Cys206Gly
ENST00000510817.2:c.616T>G	ENSP00000427455.2:p.Cys206Gly
ENST00000511886.5:n.622T>G
ENST00000511886.6:n.1558T>G
ENST00000512606.5:n.541T>G
ENST00000512606.6:n.852T>G
ENST00000514119.5:n.1053T>G
ENST00000514119.6:n.835T>G
ENST00000515507.5:n.662T>G
ENST00000650883.1:c.*33T>G	ENSP00000499142.1:n.*33T>G
ENST00000651565.1:c.259T>G	ENSP00000498768.1:p.Cys87Gly
ENST00000651699.1:c.616T>G	ENSP00000499166.1:p.Cys206Gly
ENST00000652110.1:c.616T>G	ENSP00000498513.1:p.Cys206Gly
ENST00000652271.1:c.616T>G	ENSP00000498596.1:p.Cys206Gly
ENST00000652293.1:n.1424T>G
ENST00000652543.1:c.259T>G	ENSP00000498683.1:p.Cys87Gly
ENST00000652640.1:n.1190T>G
XM_005268445.2:c.616T>G	XP_005268502.1:p.Cys206Gly
XM_005268445.4:c.616T>G	XP_005268502.1:p.Cys206Gly
XM_011537639.1:c.616T>G	XP_011535941.1:p.Cys206Gly
XM_011537639.3:c.616T>G	XP_011535941.1:p.Cys206Gly
XM_011537640.1:c.259T>G	XP_011535942.1:p.Cys87Gly
XM_011537640.2:c.259T>G	XP_011535942.1:p.Cys87Gly