Canonical Allele Identifier: CA376881710
Gene: STOX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68885534G>T , CM000672.2:g.68885534G>T GRCh38
NC_000010.10:g.70645290G>T , CM000672.1:g.70645290G>T GRCh37
NC_000010.9:g.70315296G>T NCBI36
NG_012975.1:g.62997G>T
NG_012975.2:g.62998G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000298596.11:c.1738G>T MANE Select ENSP00000298596.6:p.Gly580Cys
ENST00000642869.1:c.2074G>T ENSP00000494558.1:p.Gly692Cys
ENST00000298596.10:c.1738G>T ENSP00000298596.6:p.Gly580Cys
ENST00000399162.2:c.463+3424G>T ENSP00000382115.2:n.463+3424G>T
ENST00000399165.8:c.663+1075G>T ENSP00000382118.4:n.663+1075G>T
ENST00000399169.8:c.1738G>T ENSP00000382121.4:p.Gly580Cys
NM_001130159.2:c.663+1075G>T NP_001123631.1:n.663+1075G>T
NM_001130160.2:c.463+3424G>T NP_001123632.1:n.463+3424G>T
NM_001130161.2:c.1738G>T NP_001123633.1:p.Gly580Cys
NM_152709.4:c.1738G>T NP_689922.3:p.Gly580Cys
XM_011539454.1:c.1408G>T XP_011537756.1:p.Gly470Cys
XM_011539454.2:c.1408G>T XP_011537756.1:p.Gly470Cys
NM_152709.5:c.1738G>T MANE Select NP_689922.3:p.Gly580Cys
NM_001130161.3:c.1738G>T NP_001123633.1:p.Gly580Cys
NM_001130159.3:c.663+1075G>T NP_001123631.1:n.663+1075G>T
NM_001130160.3:c.463+3424G>T NP_001123632.1:n.463+3424G>T
NM_001130161.4:c.1738G>T NP_001123633.1:p.Gly580Cys