Canonical Allele Identifier: CA376881471
Gene: STOX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68885430G>A , CM000672.2:g.68885430G>A GRCh38
NC_000010.10:g.70645186G>A , CM000672.1:g.70645186G>A GRCh37
NC_000010.9:g.70315192G>A NCBI36
NG_012975.1:g.62893G>A
NG_012975.2:g.62894G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000298596.11:c.1634G>A MANE Select ENSP00000298596.6:p.Gly545Asp
ENST00000642869.1:c.1970G>A ENSP00000494558.1:p.Gly657Asp
ENST00000298596.10:c.1634G>A ENSP00000298596.6:p.Gly545Asp
ENST00000399162.2:c.463+3320G>A ENSP00000382115.2:n.463+3320G>A
ENST00000399165.8:c.663+971G>A ENSP00000382118.4:n.663+971G>A
ENST00000399169.8:c.1634G>A ENSP00000382121.4:p.Gly545Asp
NM_001130159.2:c.663+971G>A NP_001123631.1:n.663+971G>A
NM_001130160.2:c.463+3320G>A NP_001123632.1:n.463+3320G>A
NM_001130161.2:c.1634G>A NP_001123633.1:p.Gly545Asp
NM_152709.4:c.1634G>A NP_689922.3:p.Gly545Asp
XM_011539454.1:c.1304G>A XP_011537756.1:p.Gly435Asp
XM_011539454.2:c.1304G>A XP_011537756.1:p.Gly435Asp
NM_152709.5:c.1634G>A MANE Select NP_689922.3:p.Gly545Asp
NM_001130161.3:c.1634G>A NP_001123633.1:p.Gly545Asp
NM_001130159.3:c.663+971G>A NP_001123631.1:n.663+971G>A
NM_001130160.3:c.463+3320G>A NP_001123632.1:n.463+3320G>A
NM_001130161.4:c.1634G>A NP_001123633.1:p.Gly545Asp