Canonical Allele Identifier: CA3435285

Gene: STING1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139477323C>A , CM000667.2:g.139477323C>A	GRCh38
NC_000005.9:g.138856908C>A , CM000667.1:g.138856908C>A	GRCh37
NC_000005.8:g.138837092C>A	NCBI36
NG_034249.1:g.10468G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_198282.4:c.946+6G>T MANE Select	NP_938023.1:n.946+6G>T
ENST00000330794.9:c.946+6G>T MANE Select	ENSP00000331288.4:n.946+6G>T
NM_001301738.1:c.760-869G>T	NP_001288667.1:n.760-869G>T
NM_001301738.2:c.760-869G>T	NP_001288667.1:n.760-869G>T
NM_001367258.1:c.589+6G>T	NP_001354187.1:n.589+6G>T
NM_198282.3:c.946+6G>T	NP_938023.1:n.946+6G>T
ENST00000330794.8:c.946+6G>T	ENSP00000331288.4:n.946+6G>T
ENST00000502362.2:n.1721+6G>T
ENST00000503287.5:n.838+6G>T
ENST00000507297.5:n.2279+6G>T
ENST00000509573.5:n.559-869G>T
ENST00000510817.2:c.760-869G>T	ENSP00000427455.2:n.760-869G>T
ENST00000511886.6:n.2052+6G>T
ENST00000512606.5:n.685-869G>T
ENST00000512606.6:n.1182+6G>T
ENST00000514119.6:n.979-869G>T
ENST00000650883.1:c.*363+6G>T	ENSP00000499142.1:n.*363+6G>T
ENST00000651565.1:c.589+6G>T	ENSP00000498768.1:n.589+6G>T
ENST00000651699.1:c.946+6G>T	ENSP00000499166.1:n.946+6G>T
ENST00000652110.1:c.760-869G>T	ENSP00000498513.1:n.760-869G>T
ENST00000652271.1:c.946+6G>T	ENSP00000498596.1:n.946+6G>T
ENST00000652293.1:n.1754+6G>T
ENST00000652543.1:c.403-869G>T	ENSP00000498683.1:n.403-869G>T
ENST00000652640.1:n.1334-869G>T
XM_005268445.2:c.760-869G>T	XP_005268502.1:n.760-869G>T
XM_005268445.4:c.760-869G>T	XP_005268502.1:n.760-869G>T
XM_011537640.1:c.589+6G>T	XP_011535942.1:n.589+6G>T
XM_011537640.2:c.589+6G>T	XP_011535942.1:n.589+6G>T