Canonical Allele Identifier: CA1917550066
Gene: STOX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68885639G= , CM000672.2:g.68885639G= GRCh38
NC_000010.10:g.70645395G= , CM000672.1:g.70645395G= GRCh37
NC_000010.9:g.70315401G= NCBI36
NG_012975.1:g.63102G=
NG_012975.2:g.63103G=

Transcript Alleles

HGVS Amino-acid change
ENST00000298596.11:c.1843G= MANE Select ENSP00000298596.6:p.Glu615=
ENST00000642869.1:c.2179G= ENSP00000494558.1:p.Glu727=
ENST00000298596.10:c.1843G= ENSP00000298596.6:p.Glu615=
ENST00000399162.2:c.463+3529G= ENSP00000382115.2:n.463+3529G=
ENST00000399165.8:c.663+1180G= ENSP00000382118.4:n.663+1180G=
ENST00000399169.8:c.1843G= ENSP00000382121.4:p.Glu615=
NM_001130159.2:c.663+1180G= NP_001123631.1:n.663+1180G=
NM_001130160.2:c.463+3529G= NP_001123632.1:n.463+3529G=
NM_001130161.2:c.1843G= NP_001123633.1:p.Glu615=
NM_152709.4:c.1843G= NP_689922.3:p.Glu615=
XM_011539454.1:c.1513G= XP_011537756.1:p.Glu505=
XM_011539454.2:c.1513G= XP_011537756.1:p.Glu505=
NM_152709.5:c.1843G= MANE Select NP_689922.3:p.Glu615=
NM_001130161.3:c.1843G= NP_001123633.1:p.Glu615=
NM_001130159.3:c.663+1180G= NP_001123631.1:n.663+1180G=
NM_001130160.3:c.463+3529G= NP_001123632.1:n.463+3529G=
NM_001130161.4:c.1843G= NP_001123633.1:p.Glu615=