Canonical Allele Identifier: CA3435314

Gene: STING1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139477518A>G , CM000667.2:g.139477518A>G	GRCh38
NC_000005.9:g.138857103A>G , CM000667.1:g.138857103A>G	GRCh37
NC_000005.8:g.138837287A>G	NCBI36
NG_034249.1:g.10273T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_198282.4:c.760-3T>C MANE Select	NP_938023.1:n.760-3T>C
ENST00000330794.9:c.760-3T>C MANE Select	ENSP00000331288.4:n.760-3T>C
NM_001301738.1:c.759+752T>C	NP_001288667.1:n.759+752T>C
NM_001301738.2:c.759+752T>C	NP_001288667.1:n.759+752T>C
NM_001367258.1:c.403-3T>C	NP_001354187.1:n.403-3T>C
NM_198282.3:c.760-3T>C	NP_938023.1:n.760-3T>C
ENST00000330794.8:c.760-3T>C	ENSP00000331288.4:n.760-3T>C
ENST00000502362.2:n.1535-3T>C
ENST00000502825.1:n.538-3T>C
ENST00000503287.5:n.652-3T>C
ENST00000507297.5:n.2093-3T>C
ENST00000509573.5:n.558+752T>C
ENST00000510817.2:c.759+752T>C	ENSP00000427455.2:n.759+752T>C
ENST00000511886.5:n.766-3T>C
ENST00000511886.6:n.1866-3T>C
ENST00000512606.5:n.684+752T>C
ENST00000512606.6:n.996-3T>C
ENST00000514119.6:n.978+752T>C
ENST00000650883.1:c.*177-3T>C	ENSP00000499142.1:n.*177-3T>C
ENST00000651565.1:c.403-3T>C	ENSP00000498768.1:n.403-3T>C
ENST00000651699.1:c.760-3T>C	ENSP00000499166.1:n.760-3T>C
ENST00000652110.1:c.759+752T>C	ENSP00000498513.1:n.759+752T>C
ENST00000652271.1:c.760-3T>C	ENSP00000498596.1:n.760-3T>C
ENST00000652293.1:n.1568-3T>C
ENST00000652543.1:c.402+752T>C	ENSP00000498683.1:n.402+752T>C
ENST00000652640.1:n.1333+752T>C
XM_005268445.2:c.759+752T>C	XP_005268502.1:n.759+752T>C
XM_005268445.4:c.759+752T>C	XP_005268502.1:n.759+752T>C
XM_011537640.1:c.403-3T>C	XP_011535942.1:n.403-3T>C
XM_011537640.2:c.403-3T>C	XP_011535942.1:n.403-3T>C