Canonical Allele Identifier: CA412024315

Gene: ANOS1

Linked Data

• dbSNP Id: rs1932981633
• gnomAD v3: X-8731861-G-A
• gnomAD v4: X-8731861-G-A
• MyVariant Identifiers: chrX:g.8699902G>A (hg19) ; chrX:g.8731861G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.8731861G>A , CM000685.2:g.8731861G>A	GRCh38
NC_000023.10:g.8699902G>A , CM000685.1:g.8699902G>A	GRCh37
NC_000023.9:g.8659902G>A	NCBI36
NG_007088.1:g.5326C>T
NG_007088.2:g.5326C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262648.8:c.176C>T MANE Select	ENSP00000262648.3:p.Thr59Ile
ENST00000262648.7:c.176C>T	ENSP00000262648.3:p.Thr59Ile
ENST00000619786.1:c.173C>T	ENSP00000478734.1:p.Thr58Ile
NM_000216.2:c.176C>T	NP_000207.2:p.Thr59Ile
XM_005274501.3:c.176C>T	XP_005274558.1:p.Thr59Ile
NM_000216.3:c.176C>T	NP_000207.2:p.Thr59Ile
XM_005274501.4:c.176C>T	XP_005274558.1:p.Thr59Ile
NM_000216.4:c.176C>T MANE Select	NP_000207.2:p.Thr59Ile