Canonical Allele Identifier: CA412024281

Gene: ANOS1

Linked Data

• MyVariant Identifiers: chrX:g.8699885A>T (hg19) ; chrX:g.8731844A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.8731844A>T , CM000685.2:g.8731844A>T	GRCh38
NC_000023.10:g.8699885A>T , CM000685.1:g.8699885A>T	GRCh37
NC_000023.9:g.8659885A>T	NCBI36
NG_007088.1:g.5343T>A
NG_007088.2:g.5343T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262648.8:c.193T>A MANE Select	ENSP00000262648.3:p.Phe65Ile
ENST00000262648.7:c.193T>A	ENSP00000262648.3:p.Phe65Ile
ENST00000619786.1:c.190T>A	ENSP00000478734.1:p.Phe64Ile
NM_000216.2:c.193T>A	NP_000207.2:p.Phe65Ile
XM_005274501.3:c.193T>A	XP_005274558.1:p.Phe65Ile
NM_000216.3:c.193T>A	NP_000207.2:p.Phe65Ile
XM_005274501.4:c.193T>A	XP_005274558.1:p.Phe65Ile
NM_000216.4:c.193T>A MANE Select	NP_000207.2:p.Phe65Ile