Canonical Allele Identifier: CA515172540
Gene: ANOS1 HGNC NCBI

Linked Data

gnomAD v4: X-8732013-C-T
MyVariant Identifiers: chrX:g.8700054C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8732013C>T , CM000685.2:g.8732013C>T GRCh38
NC_000023.10:g.8700054C>T , CM000685.1:g.8700054C>T GRCh37
NC_000023.9:g.8660054C>T NCBI36
NG_007088.1:g.5174G>A
NG_007088.2:g.5174G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262648.8:c.24G>A MANE Select ENSP00000262648.3:p.Ala8=
ENST00000262648.7:c.24G>A ENSP00000262648.3:p.Ala8=
ENST00000619786.1:c.24G>A ENSP00000478734.1:p.Ala8=
NM_000216.2:c.24G>A NP_000207.2:p.Ala8=
XM_005274501.3:c.24G>A XP_005274558.1:p.Ala8=
NM_000216.3:c.24G>A NP_000207.2:p.Ala8=
XM_005274501.4:c.24G>A XP_005274558.1:p.Ala8=
NM_000216.4:c.24G>A MANE Select NP_000207.2:p.Ala8=