Canonical Allele Identifier: CA446734221

Gene: STING1

Linked Data

• MyVariant Identifiers: chr5:g.138860436G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139480851G>A , CM000667.2:g.139480851G>A	GRCh38
NC_000005.9:g.138860436G>A , CM000667.1:g.138860436G>A	GRCh37
NC_000005.8:g.138840620G>A	NCBI36
NG_034249.1:g.6940C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330794.9:c.459C>T MANE Select	ENSP00000331288.4:p.Phe153=
ENST00000502362.2:n.1234C>T
ENST00000510817.2:c.459C>T	ENSP00000427455.2:p.Phe153=
ENST00000511886.6:n.1401C>T
ENST00000512606.6:n.695C>T
ENST00000514119.6:n.678C>T
ENST00000650883.1:c.102C>T	ENSP00000499142.1:p.Phe34=
ENST00000651565.1:c.102C>T	ENSP00000498768.1:p.Phe34=
ENST00000651699.1:c.459C>T	ENSP00000499166.1:p.Phe153=
ENST00000652110.1:c.459C>T	ENSP00000498513.1:p.Phe153=
ENST00000652271.1:c.459C>T	ENSP00000498596.1:p.Phe153=
ENST00000652543.1:c.102C>T	ENSP00000498683.1:p.Phe34=
ENST00000330794.8:c.459C>T	ENSP00000331288.4:p.Phe153=
ENST00000502825.1:n.237C>T
ENST00000503287.5:n.351C>T
ENST00000503838.1:n.499C>T
ENST00000507297.5:n.1096C>T
ENST00000509573.5:n.258C>T
ENST00000510817.1:c.459C>T	ENSP00000427455.1:p.Phe153=
ENST00000511850.1:n.681C>T
ENST00000511886.5:n.465C>T
ENST00000512606.5:n.384C>T
ENST00000514119.5:n.896C>T
ENST00000515507.5:n.505C>T
NM_001301738.1:c.459C>T	NP_001288667.1:p.Phe153=
NM_198282.3:c.459C>T	NP_938023.1:p.Phe153=
XM_005268445.2:c.459C>T	XP_005268502.1:p.Phe153=
XM_011537639.1:c.459C>T	XP_011535941.1:p.Phe153=
XM_011537640.1:c.102C>T	XP_011535942.1:p.Phe34=
XM_005268445.4:c.459C>T	XP_005268502.1:p.Phe153=
XM_011537639.3:c.459C>T	XP_011535941.1:p.Phe153=
XM_011537640.2:c.102C>T	XP_011535942.1:p.Phe34=
NM_001301738.2:c.459C>T	NP_001288667.1:p.Phe153=
NM_001367258.1:c.102C>T	NP_001354187.1:p.Phe34=
NM_198282.4:c.459C>T MANE Select	NP_938023.1:p.Phe153=