Canonical Allele Identifier: CA470274102

Gene: STOX1

Linked Data

• MyVariant Identifiers: chr10:g.70645388A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68885632A>C , CM000672.2:g.68885632A>C	GRCh38
NC_000010.10:g.70645388A>C , CM000672.1:g.70645388A>C	GRCh37
NC_000010.9:g.70315394A>C	NCBI36
NG_012975.1:g.63095A>C
NG_012975.2:g.63096A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000298596.11:c.1836A>C MANE Select	ENSP00000298596.6:p.Gly612=
ENST00000642869.1:c.2172A>C	ENSP00000494558.1:p.Gly724=
ENST00000298596.10:c.1836A>C	ENSP00000298596.6:p.Gly612=
ENST00000399162.2:c.463+3522A>C	ENSP00000382115.2:n.463+3522A>C
ENST00000399165.8:c.663+1173A>C	ENSP00000382118.4:n.663+1173A>C
ENST00000399169.8:c.1836A>C	ENSP00000382121.4:p.Gly612=
NM_001130159.2:c.663+1173A>C	NP_001123631.1:n.663+1173A>C
NM_001130160.2:c.463+3522A>C	NP_001123632.1:n.463+3522A>C
NM_001130161.2:c.1836A>C	NP_001123633.1:p.Gly612=
NM_152709.4:c.1836A>C	NP_689922.3:p.Gly612=
XM_011539454.1:c.1506A>C	XP_011537756.1:p.Gly502=
XM_011539454.2:c.1506A>C	XP_011537756.1:p.Gly502=
NM_152709.5:c.1836A>C MANE Select	NP_689922.3:p.Gly612=
NM_001130161.3:c.1836A>C	NP_001123633.1:p.Gly612=
NM_001130159.3:c.663+1173A>C	NP_001123631.1:n.663+1173A>C
NM_001130160.3:c.463+3522A>C	NP_001123632.1:n.463+3522A>C
NM_001130161.4:c.1836A>C	NP_001123633.1:p.Gly612=