Canonical Allele Identifier: CA412024670

Gene: ANOS1

Linked Data

• gnomAD v4: X-8732000-A-G
• MyVariant Identifiers: chrX:g.8700041A>G (hg19) ; chrX:g.8732000A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.8732000A>G , CM000685.2:g.8732000A>G	GRCh38
NC_000023.10:g.8700041A>G , CM000685.1:g.8700041A>G	GRCh37
NC_000023.9:g.8660041A>G	NCBI36
NG_007088.1:g.5187T>C
NG_007088.2:g.5187T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262648.8:c.37T>C MANE Select	ENSP00000262648.3:p.Cys13Arg
ENST00000262648.7:c.37T>C	ENSP00000262648.3:p.Cys13Arg
ENST00000619786.1:c.37T>C	ENSP00000478734.1:p.Cys13Arg
NM_000216.2:c.37T>C	NP_000207.2:p.Cys13Arg
XM_005274501.3:c.37T>C	XP_005274558.1:p.Cys13Arg
NM_000216.3:c.37T>C	NP_000207.2:p.Cys13Arg
XM_005274501.4:c.37T>C	XP_005274558.1:p.Cys13Arg
NM_000216.4:c.37T>C MANE Select	NP_000207.2:p.Cys13Arg