Canonical Allele Identifier: CA1917550034

Gene: STOX1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68885555C= , CM000672.2:g.68885555C=	GRCh38
NC_000010.10:g.70645311C= , CM000672.1:g.70645311C=	GRCh37
NC_000010.9:g.70315317C=	NCBI36
NG_012975.1:g.63018C=
NG_012975.2:g.63019C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298596.11:c.1759C= MANE Select	ENSP00000298596.6:p.Gln587=
ENST00000642869.1:c.2095C=	ENSP00000494558.1:p.Gln699=
ENST00000298596.10:c.1759C=	ENSP00000298596.6:p.Gln587=
ENST00000399162.2:c.463+3445C=	ENSP00000382115.2:n.463+3445C=
ENST00000399165.8:c.663+1096C=	ENSP00000382118.4:n.663+1096C=
ENST00000399169.8:c.1759C=	ENSP00000382121.4:p.Gln587=
NM_001130159.2:c.663+1096C=	NP_001123631.1:n.663+1096C=
NM_001130160.2:c.463+3445C=	NP_001123632.1:n.463+3445C=
NM_001130161.2:c.1759C=	NP_001123633.1:p.Gln587=
NM_152709.4:c.1759C=	NP_689922.3:p.Gln587=
XM_011539454.1:c.1429C=	XP_011537756.1:p.Gln477=
XM_011539454.2:c.1429C=	XP_011537756.1:p.Gln477=
NM_152709.5:c.1759C= MANE Select	NP_689922.3:p.Gln587=
NM_001130161.3:c.1759C=	NP_001123633.1:p.Gln587=
NM_001130159.3:c.663+1096C=	NP_001123631.1:n.663+1096C=
NM_001130160.3:c.463+3445C=	NP_001123632.1:n.463+3445C=
NM_001130161.4:c.1759C=	NP_001123633.1:p.Gln587=