Canonical Allele Identifier: CA929584291
Gene: STOX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68859163G>C , CM000672.2:g.68859163G>C GRCh38
NC_000010.10:g.70618919G>C , CM000672.1:g.70618919G>C GRCh37
NC_000010.9:g.70288925G>C NCBI36
NG_012975.1:g.36626G>C
NG_012975.2:g.36627G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000298596.11:c.311-22795G>C MANE Select ENSP00000298596.6:n.311-22795G>C
ENST00000642869.1:c.647-22795G>C ENSP00000494558.1:n.647-22795G>C
ENST00000298596.10:c.311-22795G>C ENSP00000298596.6:n.311-22795G>C
ENST00000399162.2:c.311-22795G>C ENSP00000382115.2:n.311-22795G>C
ENST00000399165.8:c.311-22795G>C ENSP00000382118.4:n.311-22795G>C
ENST00000399169.8:c.311-22795G>C ENSP00000382121.4:n.311-22795G>C
NM_001130159.2:c.311-22795G>C NP_001123631.1:n.311-22795G>C
NM_001130160.2:c.311-22795G>C NP_001123632.1:n.311-22795G>C
NM_001130161.2:c.311-22795G>C NP_001123633.1:n.311-22795G>C
NM_152709.4:c.311-22795G>C NP_689922.3:n.311-22795G>C
XM_011539454.1:c.-20-22795G>C XP_011537756.1:n.-20-22795G>C
XM_011539454.2:c.-20-22795G>C XP_011537756.1:n.-20-22795G>C
NM_152709.5:c.311-22795G>C MANE Select NP_689922.3:n.311-22795G>C
NM_001130161.3:c.311-22795G>C NP_001123633.1:n.311-22795G>C
NM_001130159.3:c.311-22795G>C NP_001123631.1:n.311-22795G>C
NM_001130160.3:c.311-22795G>C NP_001123632.1:n.311-22795G>C
NM_001130161.4:c.311-22795G>C NP_001123633.1:n.311-22795G>C