Canonical Allele Identifier: CA879152631

Gene: ANOS1

Linked Data

• dbSNP Id: rs1252893321
• gnomAD v3: X-8587721-T-A
• gnomAD v4: X-8587721-T-A
• MyVariant Identifiers: chrX:g.8555762T>A (hg19) ; chrX:g.8587721T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.8587721T>A , CM000685.2:g.8587721T>A	GRCh38
NC_000023.10:g.8555762T>A , CM000685.1:g.8555762T>A	GRCh37
NC_000023.9:g.8515762T>A	NCBI36
NG_007088.1:g.149466A>T
NG_007088.2:g.149466A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000262648.8:c.726+73A>T MANE Select	ENSP00000262648.3:n.726+73A>T
ENST00000262648.7:c.726+73A>T	ENSP00000262648.3:n.726+73A>T
ENST00000619786.1:c.723+73A>T	ENSP00000478734.1:n.723+73A>T
NM_000216.2:c.726+73A>T	NP_000207.2:n.726+73A>T
XM_005274501.3:c.726+73A>T	XP_005274558.1:n.726+73A>T
NM_000216.3:c.726+73A>T	NP_000207.2:n.726+73A>T
XM_005274501.4:c.726+73A>T	XP_005274558.1:n.726+73A>T
NM_000216.4:c.726+73A>T MANE Select	NP_000207.2:n.726+73A>T