Canonical Allele Identifier: CA1917550061
Gene: STOX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68885624T= , CM000672.2:g.68885624T= GRCh38
NC_000010.10:g.70645380T= , CM000672.1:g.70645380T= GRCh37
NC_000010.9:g.70315386T= NCBI36
NG_012975.1:g.63087T=
NG_012975.2:g.63088T=

Transcript Alleles

HGVS Amino-acid change
ENST00000298596.11:c.1828T= MANE Select ENSP00000298596.6:p.Tyr610=
ENST00000642869.1:c.2164T= ENSP00000494558.1:p.Tyr722=
ENST00000298596.10:c.1828T= ENSP00000298596.6:p.Tyr610=
ENST00000399162.2:c.463+3514T= ENSP00000382115.2:n.463+3514T=
ENST00000399165.8:c.663+1165T= ENSP00000382118.4:n.663+1165T=
ENST00000399169.8:c.1828T= ENSP00000382121.4:p.Tyr610=
NM_001130159.2:c.663+1165T= NP_001123631.1:n.663+1165T=
NM_001130160.2:c.463+3514T= NP_001123632.1:n.463+3514T=
NM_001130161.2:c.1828T= NP_001123633.1:p.Tyr610=
NM_152709.4:c.1828T= NP_689922.3:p.Tyr610=
XM_011539454.1:c.1498T= XP_011537756.1:p.Tyr500=
XM_011539454.2:c.1498T= XP_011537756.1:p.Tyr500=
NM_152709.5:c.1828T= MANE Select NP_689922.3:p.Tyr610=
NM_001130161.3:c.1828T= NP_001123633.1:p.Tyr610=
NM_001130159.3:c.663+1165T= NP_001123631.1:n.663+1165T=
NM_001130160.3:c.463+3514T= NP_001123632.1:n.463+3514T=
NM_001130161.4:c.1828T= NP_001123633.1:p.Tyr610=