Canonical Allele Identifier: CA412023871

Gene: ANOS1

Linked Data

• MyVariant Identifiers: chrX:g.8555863T>G (hg19) ; chrX:g.8587822T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.8587822T>G , CM000685.2:g.8587822T>G	GRCh38
NC_000023.10:g.8555863T>G , CM000685.1:g.8555863T>G	GRCh37
NC_000023.9:g.8515863T>G	NCBI36
NG_007088.1:g.149365A>C
NG_007088.2:g.149365A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000262648.8:c.698A>C MANE Select	ENSP00000262648.3:p.Asp233Ala
ENST00000262648.7:c.698A>C	ENSP00000262648.3:p.Asp233Ala
ENST00000619786.1:c.695A>C	ENSP00000478734.1:p.Asp232Ala
NM_000216.2:c.698A>C	NP_000207.2:p.Asp233Ala
XM_005274501.3:c.698A>C	XP_005274558.1:p.Asp233Ala
NM_000216.3:c.698A>C	NP_000207.2:p.Asp233Ala
XM_005274501.4:c.698A>C	XP_005274558.1:p.Asp233Ala
NM_000216.4:c.698A>C MANE Select	NP_000207.2:p.Asp233Ala