Canonical Allele Identifier: CA1586315497

Gene: STING1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139480771G= , CM000667.2:g.139480771G=	GRCh38
NC_000005.9:g.138860356G= , CM000667.1:g.138860356G=	GRCh37
NC_000005.8:g.138840540G=	NCBI36
NG_034249.1:g.7020C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330794.9:c.520+19C= MANE Select	ENSP00000331288.4:n.520+19C=
ENST00000502362.2:n.1295+19C=
ENST00000510817.2:c.520+19C=	ENSP00000427455.2:n.520+19C=
ENST00000511886.6:n.1462+19C=
ENST00000512606.6:n.756+19C=
ENST00000514119.6:n.739+19C=
ENST00000650883.1:c.163+19C=	ENSP00000499142.1:n.163+19C=
ENST00000651565.1:c.163+19C=	ENSP00000498768.1:n.163+19C=
ENST00000651699.1:c.520+19C=	ENSP00000499166.1:n.520+19C=
ENST00000652110.1:c.520+19C=	ENSP00000498513.1:n.520+19C=
ENST00000652271.1:c.520+19C=	ENSP00000498596.1:n.520+19C=
ENST00000652543.1:c.163+19C=	ENSP00000498683.1:n.163+19C=
ENST00000330794.8:c.520+19C=	ENSP00000331288.4:n.520+19C=
ENST00000502825.1:n.298+19C=
ENST00000503287.5:n.412+19C=
ENST00000503838.1:n.560+19C=
ENST00000507297.5:n.1157+19C=
ENST00000509573.5:n.319+19C=
ENST00000510817.1:c.520+19C=	ENSP00000427455.1:n.520+19C=
ENST00000511850.1:n.742+19C=
ENST00000511886.5:n.526+19C=
ENST00000512606.5:n.445+19C=
ENST00000514119.5:n.957+19C=
ENST00000515507.5:n.566+19C=
NM_001301738.1:c.520+19C=	NP_001288667.1:n.520+19C=
NM_198282.3:c.520+19C=	NP_938023.1:n.520+19C=
XM_005268445.2:c.520+19C=	XP_005268502.1:n.520+19C=
XM_011537639.1:c.520+19C=	XP_011535941.1:n.520+19C=
XM_011537640.1:c.163+19C=	XP_011535942.1:n.163+19C=
XM_005268445.4:c.520+19C=	XP_005268502.1:n.520+19C=
XM_011537639.3:c.520+19C=	XP_011535941.1:n.520+19C=
XM_011537640.2:c.163+19C=	XP_011535942.1:n.163+19C=
NM_001301738.2:c.520+19C=	NP_001288667.1:n.520+19C=
NM_001367258.1:c.163+19C=	NP_001354187.1:n.163+19C=
NM_198282.4:c.520+19C= MANE Select	NP_938023.1:n.520+19C=