Canonical Allele Identifier: CA412024263

Gene: ANOS1

Linked Data

• MyVariant Identifiers: chrX:g.8699879G>A (hg19) ; chrX:g.8731838G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.8731838G>A , CM000685.2:g.8731838G>A	GRCh38
NC_000023.10:g.8699879G>A , CM000685.1:g.8699879G>A	GRCh37
NC_000023.9:g.8659879G>A	NCBI36
NG_007088.1:g.5349C>T
NG_007088.2:g.5349C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262648.8:c.199C>T MANE Select	ENSP00000262648.3:p.His67Tyr
ENST00000262648.7:c.199C>T	ENSP00000262648.3:p.His67Tyr
ENST00000619786.1:c.196C>T	ENSP00000478734.1:p.His66Tyr
NM_000216.2:c.199C>T	NP_000207.2:p.His67Tyr
XM_005274501.3:c.199C>T	XP_005274558.1:p.His67Tyr
NM_000216.3:c.199C>T	NP_000207.2:p.His67Tyr
XM_005274501.4:c.199C>T	XP_005274558.1:p.His67Tyr
NM_000216.4:c.199C>T MANE Select	NP_000207.2:p.His67Tyr