Canonical Allele Identifier: CA361481054

Gene: STING1

Linked Data

• MyVariant Identifiers: chr5:g.138860441T>C (hg19) ; chr5:g.139480856T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139480856T>C , CM000667.2:g.139480856T>C	GRCh38
NC_000005.9:g.138860441T>C , CM000667.1:g.138860441T>C	GRCh37
NC_000005.8:g.138840625T>C	NCBI36
NG_034249.1:g.6935A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330794.9:c.454A>G MANE Select	ENSP00000331288.4:p.Asn152Asp
ENST00000502362.2:n.1229A>G
ENST00000510817.2:c.454A>G	ENSP00000427455.2:p.Asn152Asp
ENST00000511886.6:n.1396A>G
ENST00000512606.6:n.690A>G
ENST00000514119.6:n.673A>G
ENST00000650883.1:c.97A>G	ENSP00000499142.1:p.Asn33Asp
ENST00000651565.1:c.97A>G	ENSP00000498768.1:p.Asn33Asp
ENST00000651699.1:c.454A>G	ENSP00000499166.1:p.Asn152Asp
ENST00000652110.1:c.454A>G	ENSP00000498513.1:p.Asn152Asp
ENST00000652271.1:c.454A>G	ENSP00000498596.1:p.Asn152Asp
ENST00000652543.1:c.97A>G	ENSP00000498683.1:p.Asn33Asp
ENST00000330794.8:c.454A>G	ENSP00000331288.4:p.Asn152Asp
ENST00000502825.1:n.232A>G
ENST00000503287.5:n.346A>G
ENST00000503838.1:n.494A>G
ENST00000507297.5:n.1091A>G
ENST00000509573.5:n.253A>G
ENST00000510817.1:c.454A>G	ENSP00000427455.1:p.Asn152Asp
ENST00000511850.1:n.676A>G
ENST00000511886.5:n.460A>G
ENST00000512606.5:n.379A>G
ENST00000514119.5:n.891A>G
ENST00000515507.5:n.500A>G
NM_001301738.1:c.454A>G	NP_001288667.1:p.Asn152Asp
NM_198282.3:c.454A>G	NP_938023.1:p.Asn152Asp
XM_005268445.2:c.454A>G	XP_005268502.1:p.Asn152Asp
XM_011537639.1:c.454A>G	XP_011535941.1:p.Asn152Asp
XM_011537640.1:c.97A>G	XP_011535942.1:p.Asn33Asp
XM_005268445.4:c.454A>G	XP_005268502.1:p.Asn152Asp
XM_011537639.3:c.454A>G	XP_011535941.1:p.Asn152Asp
XM_011537640.2:c.97A>G	XP_011535942.1:p.Asn33Asp
NM_001301738.2:c.454A>G	NP_001288667.1:p.Asn152Asp
NM_001367258.1:c.97A>G	NP_001354187.1:p.Asn33Asp
NM_198282.4:c.454A>G MANE Select	NP_938023.1:p.Asn152Asp