Canonical Allele Identifier: CA412024396
Gene: ANOS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.8699937A>T (hg19) chrX:g.8731896A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8731896A>T , CM000685.2:g.8731896A>T GRCh38
NC_000023.10:g.8699937A>T , CM000685.1:g.8699937A>T GRCh37
NC_000023.9:g.8659937A>T NCBI36
NG_007088.1:g.5291T>A
NG_007088.2:g.5291T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262648.8:c.141T>A MANE Select ENSP00000262648.3:p.Ala47=
ENST00000262648.7:c.141T>A ENSP00000262648.3:p.Ala47=
ENST00000619786.1:c.139T>A ENSP00000478734.1:p.Ser47Thr
NM_000216.2:c.141T>A NP_000207.2:p.Ala47=
XM_005274501.3:c.141T>A XP_005274558.1:p.Ala47=
NM_000216.3:c.141T>A NP_000207.2:p.Ala47=
XM_005274501.4:c.141T>A XP_005274558.1:p.Ala47=
NM_000216.4:c.141T>A MANE Select NP_000207.2:p.Ala47=
Search 100 bp 5'
Search 100 bp 3'