Canonical Allele Identifier: CA412023840

Gene: ANOS1

Linked Data

• COSMIC: COSM6383595
• MyVariant Identifiers: chrX:g.8555850C>A (hg19) ; chrX:g.8587809C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.8587809C>A , CM000685.2:g.8587809C>A	GRCh38
NC_000023.10:g.8555850C>A , CM000685.1:g.8555850C>A	GRCh37
NC_000023.9:g.8515850C>A	NCBI36
NG_007088.1:g.149378G>T
NG_007088.2:g.149378G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000262648.8:c.711G>T MANE Select	ENSP00000262648.3:p.Trp237Cys
ENST00000262648.7:c.711G>T	ENSP00000262648.3:p.Trp237Cys
ENST00000619786.1:c.708G>T	ENSP00000478734.1:p.Trp236Cys
NM_000216.2:c.711G>T	NP_000207.2:p.Trp237Cys
XM_005274501.3:c.711G>T	XP_005274558.1:p.Trp237Cys
NM_000216.3:c.711G>T	NP_000207.2:p.Trp237Cys
XM_005274501.4:c.711G>T	XP_005274558.1:p.Trp237Cys
NM_000216.4:c.711G>T MANE Select	NP_000207.2:p.Trp237Cys