Canonical Allele Identifier: CA376881467

Gene: STOX1

Linked Data

• MyVariant Identifiers: chr10:g.70645184T>G (hg19) ; chr10:g.68885428T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68885428T>G , CM000672.2:g.68885428T>G	GRCh38
NC_000010.10:g.70645184T>G , CM000672.1:g.70645184T>G	GRCh37
NC_000010.9:g.70315190T>G	NCBI36
NG_012975.1:g.62891T>G
NG_012975.2:g.62892T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298596.11:c.1632T>G MANE Select	ENSP00000298596.6:p.Asp544Glu
ENST00000642869.1:c.1968T>G	ENSP00000494558.1:p.Asp656Glu
ENST00000298596.10:c.1632T>G	ENSP00000298596.6:p.Asp544Glu
ENST00000399162.2:c.463+3318T>G	ENSP00000382115.2:n.463+3318T>G
ENST00000399165.8:c.663+969T>G	ENSP00000382118.4:n.663+969T>G
ENST00000399169.8:c.1632T>G	ENSP00000382121.4:p.Asp544Glu
NM_001130159.2:c.663+969T>G	NP_001123631.1:n.663+969T>G
NM_001130160.2:c.463+3318T>G	NP_001123632.1:n.463+3318T>G
NM_001130161.2:c.1632T>G	NP_001123633.1:p.Asp544Glu
NM_152709.4:c.1632T>G	NP_689922.3:p.Asp544Glu
XM_011539454.1:c.1302T>G	XP_011537756.1:p.Asp434Glu
XM_011539454.2:c.1302T>G	XP_011537756.1:p.Asp434Glu
NM_152709.5:c.1632T>G MANE Select	NP_689922.3:p.Asp544Glu
NM_001130161.3:c.1632T>G	NP_001123633.1:p.Asp544Glu
NM_001130159.3:c.663+969T>G	NP_001123631.1:n.663+969T>G
NM_001130160.3:c.463+3318T>G	NP_001123632.1:n.463+3318T>G
NM_001130161.4:c.1632T>G	NP_001123633.1:p.Asp544Glu