Canonical Allele Identifier: CA361480172

Gene: STING1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139478415T>C , CM000667.2:g.139478415T>C	GRCh38
NC_000005.9:g.138858000T>C , CM000667.1:g.138858000T>C	GRCh37
NC_000005.8:g.138838184T>C	NCBI36
NG_034249.1:g.9376A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_198282.4:c.614A>G MANE Select	NP_938023.1:p.Asp205Gly
ENST00000330794.9:c.614A>G MANE Select	ENSP00000331288.4:p.Asp205Gly
NM_001301738.1:c.614A>G	NP_001288667.1:p.Asp205Gly
NM_001301738.2:c.614A>G	NP_001288667.1:p.Asp205Gly
NM_001367258.1:c.257A>G	NP_001354187.1:p.Asp86Gly
NM_198282.3:c.614A>G	NP_938023.1:p.Asp205Gly
ENST00000330794.8:c.614A>G	ENSP00000331288.4:p.Asp205Gly
ENST00000502362.2:n.1389A>G
ENST00000502825.1:n.392A>G
ENST00000503287.5:n.506A>G
ENST00000507297.5:n.1947A>G
ENST00000509573.5:n.413A>G
ENST00000510817.1:c.614A>G	ENSP00000427455.1:p.Asp205Gly
ENST00000510817.2:c.614A>G	ENSP00000427455.2:p.Asp205Gly
ENST00000511886.5:n.620A>G
ENST00000511886.6:n.1556A>G
ENST00000512606.5:n.539A>G
ENST00000512606.6:n.850A>G
ENST00000514119.5:n.1051A>G
ENST00000514119.6:n.833A>G
ENST00000515507.5:n.660A>G
ENST00000650883.1:c.*31A>G	ENSP00000499142.1:n.*31A>G
ENST00000651565.1:c.257A>G	ENSP00000498768.1:p.Asp86Gly
ENST00000651699.1:c.614A>G	ENSP00000499166.1:p.Asp205Gly
ENST00000652110.1:c.614A>G	ENSP00000498513.1:p.Asp205Gly
ENST00000652271.1:c.614A>G	ENSP00000498596.1:p.Asp205Gly
ENST00000652293.1:n.1422A>G
ENST00000652543.1:c.257A>G	ENSP00000498683.1:p.Asp86Gly
ENST00000652640.1:n.1188A>G
XM_005268445.2:c.614A>G	XP_005268502.1:p.Asp205Gly
XM_005268445.4:c.614A>G	XP_005268502.1:p.Asp205Gly
XM_011537639.1:c.614A>G	XP_011535941.1:p.Asp205Gly
XM_011537639.3:c.614A>G	XP_011535941.1:p.Asp205Gly
XM_011537640.1:c.257A>G	XP_011535942.1:p.Asp86Gly
XM_011537640.2:c.257A>G	XP_011535942.1:p.Asp86Gly