Canonical Allele Identifier: CA515172523
Gene: ANOS1 HGNC NCBI

Linked Data

gnomAD v4: X-8731995-G-T
MyVariant Identifiers: chrX:g.8700036G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8731995G>T , CM000685.2:g.8731995G>T GRCh38
NC_000023.10:g.8700036G>T , CM000685.1:g.8700036G>T GRCh37
NC_000023.9:g.8660036G>T NCBI36
NG_007088.1:g.5192C>A
NG_007088.2:g.5192C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262648.8:c.42C>A MANE Select ENSP00000262648.3:p.Leu14=
ENST00000262648.7:c.42C>A ENSP00000262648.3:p.Leu14=
ENST00000619786.1:c.42C>A ENSP00000478734.1:p.Leu14=
NM_000216.2:c.42C>A NP_000207.2:p.Leu14=
XM_005274501.3:c.42C>A XP_005274558.1:p.Leu14=
NM_000216.3:c.42C>A NP_000207.2:p.Leu14=
XM_005274501.4:c.42C>A XP_005274558.1:p.Leu14=
NM_000216.4:c.42C>A MANE Select NP_000207.2:p.Leu14=