Canonical Allele Identifier: CA515172531
Gene: ANOS1 HGNC NCBI

Linked Data

gnomAD v4: X-8732007-C-A
MyVariant Identifiers: chrX:g.8700048C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8732007C>A , CM000685.2:g.8732007C>A GRCh38
NC_000023.10:g.8700048C>A , CM000685.1:g.8700048C>A GRCh37
NC_000023.9:g.8660048C>A NCBI36
NG_007088.1:g.5180G>T
NG_007088.2:g.5180G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000262648.8:c.30G>T MANE Select ENSP00000262648.3:p.Leu10=
ENST00000262648.7:c.30G>T ENSP00000262648.3:p.Leu10=
ENST00000619786.1:c.30G>T ENSP00000478734.1:p.Leu10=
NM_000216.2:c.30G>T NP_000207.2:p.Leu10=
XM_005274501.3:c.30G>T XP_005274558.1:p.Leu10=
NM_000216.3:c.30G>T NP_000207.2:p.Leu10=
XM_005274501.4:c.30G>T XP_005274558.1:p.Leu10=
NM_000216.4:c.30G>T MANE Select NP_000207.2:p.Leu10=