Canonical Allele Identifier: CA376881719
Gene: STOX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68885538A>T , CM000672.2:g.68885538A>T GRCh38
NC_000010.10:g.70645294A>T , CM000672.1:g.70645294A>T GRCh37
NC_000010.9:g.70315300A>T NCBI36
NG_012975.1:g.63001A>T
NG_012975.2:g.63002A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000298596.11:c.1742A>T MANE Select ENSP00000298596.6:p.His581Leu
ENST00000642869.1:c.2078A>T ENSP00000494558.1:p.His693Leu
ENST00000298596.10:c.1742A>T ENSP00000298596.6:p.His581Leu
ENST00000399162.2:c.463+3428A>T ENSP00000382115.2:n.463+3428A>T
ENST00000399165.8:c.663+1079A>T ENSP00000382118.4:n.663+1079A>T
ENST00000399169.8:c.1742A>T ENSP00000382121.4:p.His581Leu
NM_001130159.2:c.663+1079A>T NP_001123631.1:n.663+1079A>T
NM_001130160.2:c.463+3428A>T NP_001123632.1:n.463+3428A>T
NM_001130161.2:c.1742A>T NP_001123633.1:p.His581Leu
NM_152709.4:c.1742A>T NP_689922.3:p.His581Leu
XM_011539454.1:c.1412A>T XP_011537756.1:p.His471Leu
XM_011539454.2:c.1412A>T XP_011537756.1:p.His471Leu
NM_152709.5:c.1742A>T MANE Select NP_689922.3:p.His581Leu
NM_001130161.3:c.1742A>T NP_001123633.1:p.His581Leu
NM_001130159.3:c.663+1079A>T NP_001123631.1:n.663+1079A>T
NM_001130160.3:c.463+3428A>T NP_001123632.1:n.463+3428A>T
NM_001130161.4:c.1742A>T NP_001123633.1:p.His581Leu