Canonical Allele Identifier: CA1917549982

Gene: STOX1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68885422_68885424delinsCTT , CM000672.2:g.68885422_68885424delinsCTT	GRCh38
NC_000010.10:g.70645178_70645180delinsCTT , CM000672.1:g.70645178_70645180delinsCTT	GRCh37
NC_000010.9:g.70315184_70315186delinsCTT	NCBI36
NG_012975.1:g.62885_62887delinsCTT
NG_012975.2:g.62886_62888delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298596.11:c.1626_1628delinsCTT MANE Select	ENSP00000298596.6:p.Ile542=
ENST00000642869.1:c.1962_1964delinsCTT	ENSP00000494558.1:p.Ile654=
ENST00000298596.10:c.1626_1628delinsCTT	ENSP00000298596.6:p.Ile542=
ENST00000399162.2:c.463+3312_463+3314delinsCTT	ENSP00000382115.2:n.463+3312_463+3314delinsCTT
ENST00000399165.8:c.663+963_663+965delinsCTT	ENSP00000382118.4:n.663+963_663+965delinsCTT
ENST00000399169.8:c.1626_1628delinsCTT	ENSP00000382121.4:p.Ile542=
NM_001130159.2:c.663+963_663+965delinsCTT	NP_001123631.1:n.663+963_663+965delinsCTT
NM_001130160.2:c.463+3312_463+3314delinsCTT	NP_001123632.1:n.463+3312_463+3314delinsCTT
NM_001130161.2:c.1626_1628delinsCTT	NP_001123633.1:p.Ile542=
NM_152709.4:c.1626_1628delinsCTT	NP_689922.3:p.Ile542=
XM_011539454.1:c.1296_1298delinsCTT	XP_011537756.1:p.Ile432=
XM_011539454.2:c.1296_1298delinsCTT	XP_011537756.1:p.Ile432=
NM_152709.5:c.1626_1628delinsCTT MANE Select	NP_689922.3:p.Ile542=
NM_001130161.3:c.1626_1628delinsCTT	NP_001123633.1:p.Ile542=
NM_001130159.3:c.663+963_663+965delinsCTT	NP_001123631.1:n.663+963_663+965delinsCTT
NM_001130160.3:c.463+3312_463+3314delinsCTT	NP_001123632.1:n.463+3312_463+3314delinsCTT
NM_001130161.4:c.1626_1628delinsCTT	NP_001123633.1:p.Ile542=