Canonical Allele Identifier: CA1586315532

Gene: STING1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139480858C= , CM000667.2:g.139480858C=	GRCh38
NC_000005.9:g.138860443C= , CM000667.1:g.138860443C=	GRCh37
NC_000005.8:g.138840627C=	NCBI36
NG_034249.1:g.6933G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330794.9:c.452G= MANE Select	ENSP00000331288.4:p.Gly151=
ENST00000502362.2:n.1227G=
ENST00000510817.2:c.452G=	ENSP00000427455.2:p.Gly151=
ENST00000511886.6:n.1394G=
ENST00000512606.6:n.688G=
ENST00000514119.6:n.671G=
ENST00000650883.1:c.95G=	ENSP00000499142.1:p.Gly32=
ENST00000651565.1:c.95G=	ENSP00000498768.1:p.Gly32=
ENST00000651699.1:c.452G=	ENSP00000499166.1:p.Gly151=
ENST00000652110.1:c.452G=	ENSP00000498513.1:p.Gly151=
ENST00000652271.1:c.452G=	ENSP00000498596.1:p.Gly151=
ENST00000652543.1:c.95G=	ENSP00000498683.1:p.Gly32=
ENST00000330794.8:c.452G=	ENSP00000331288.4:p.Gly151=
ENST00000502825.1:n.230G=
ENST00000503287.5:n.344G=
ENST00000503838.1:n.492G=
ENST00000507297.5:n.1089G=
ENST00000509573.5:n.251G=
ENST00000510817.1:c.452G=	ENSP00000427455.1:p.Gly151=
ENST00000511850.1:n.674G=
ENST00000511886.5:n.458G=
ENST00000512606.5:n.377G=
ENST00000514119.5:n.889G=
ENST00000515507.5:n.498G=
NM_001301738.1:c.452G=	NP_001288667.1:p.Gly151=
NM_198282.3:c.452G=	NP_938023.1:p.Gly151=
XM_005268445.2:c.452G=	XP_005268502.1:p.Gly151=
XM_011537639.1:c.452G=	XP_011535941.1:p.Gly151=
XM_011537640.1:c.95G=	XP_011535942.1:p.Gly32=
XM_005268445.4:c.452G=	XP_005268502.1:p.Gly151=
XM_011537639.3:c.452G=	XP_011535941.1:p.Gly151=
XM_011537640.2:c.95G=	XP_011535942.1:p.Gly32=
NM_001301738.2:c.452G=	NP_001288667.1:p.Gly151=
NM_001367258.1:c.95G=	NP_001354187.1:p.Gly32=
NM_198282.4:c.452G= MANE Select	NP_938023.1:p.Gly151=