Canonical Allele Identifier: CA470274088

Gene: STOX1

Linked Data

• MyVariant Identifiers: chr10:g.70645358A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68885602A>G , CM000672.2:g.68885602A>G	GRCh38
NC_000010.10:g.70645358A>G , CM000672.1:g.70645358A>G	GRCh37
NC_000010.9:g.70315364A>G	NCBI36
NG_012975.1:g.63065A>G
NG_012975.2:g.63066A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298596.11:c.1806A>G MANE Select	ENSP00000298596.6:p.Glu602=
ENST00000642869.1:c.2142A>G	ENSP00000494558.1:p.Glu714=
ENST00000298596.10:c.1806A>G	ENSP00000298596.6:p.Glu602=
ENST00000399162.2:c.463+3492A>G	ENSP00000382115.2:n.463+3492A>G
ENST00000399165.8:c.663+1143A>G	ENSP00000382118.4:n.663+1143A>G
ENST00000399169.8:c.1806A>G	ENSP00000382121.4:p.Glu602=
NM_001130159.2:c.663+1143A>G	NP_001123631.1:n.663+1143A>G
NM_001130160.2:c.463+3492A>G	NP_001123632.1:n.463+3492A>G
NM_001130161.2:c.1806A>G	NP_001123633.1:p.Glu602=
NM_152709.4:c.1806A>G	NP_689922.3:p.Glu602=
XM_011539454.1:c.1476A>G	XP_011537756.1:p.Glu492=
XM_011539454.2:c.1476A>G	XP_011537756.1:p.Glu492=
NM_152709.5:c.1806A>G MANE Select	NP_689922.3:p.Glu602=
NM_001130161.3:c.1806A>G	NP_001123633.1:p.Glu602=
NM_001130159.3:c.663+1143A>G	NP_001123631.1:n.663+1143A>G
NM_001130160.3:c.463+3492A>G	NP_001123632.1:n.463+3492A>G
NM_001130161.4:c.1806A>G	NP_001123633.1:p.Glu602=