Canonical Allele Identifier: CA515172457
Gene: ANOS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.8699916C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8731875C>T , CM000685.2:g.8731875C>T GRCh38
NC_000023.10:g.8699916C>T , CM000685.1:g.8699916C>T GRCh37
NC_000023.9:g.8659916C>T NCBI36
NG_007088.1:g.5312G>A
NG_007088.2:g.5312G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262648.8:c.162G>A MANE Select ENSP00000262648.3:p.Leu54=
ENST00000262648.7:c.162G>A ENSP00000262648.3:p.Leu54=
ENST00000619786.1:c.159G>A ENSP00000478734.1:p.Leu53=
NM_000216.2:c.162G>A NP_000207.2:p.Leu54=
XM_005274501.3:c.162G>A XP_005274558.1:p.Leu54=
NM_000216.3:c.162G>A NP_000207.2:p.Leu54=
XM_005274501.4:c.162G>A XP_005274558.1:p.Leu54=
NM_000216.4:c.162G>A MANE Select NP_000207.2:p.Leu54=