Canonical Allele Identifier: CA412024409
Gene: ANOS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.8699942G>C (hg19) chrX:g.8731901G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8731901G>C , CM000685.2:g.8731901G>C GRCh38
NC_000023.10:g.8699942G>C , CM000685.1:g.8699942G>C GRCh37
NC_000023.9:g.8659942G>C NCBI36
NG_007088.1:g.5286C>G
NG_007088.2:g.5286C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262648.8:c.136C>G MANE Select ENSP00000262648.3:p.Arg46Gly
ENST00000262648.7:c.136C>G ENSP00000262648.3:p.Arg46Gly
ENST00000619786.1:c.134C>G ENSP00000478734.1:p.Ala45Gly
NM_000216.2:c.136C>G NP_000207.2:p.Arg46Gly
XM_005274501.3:c.136C>G XP_005274558.1:p.Arg46Gly
NM_000216.3:c.136C>G NP_000207.2:p.Arg46Gly
XM_005274501.4:c.136C>G XP_005274558.1:p.Arg46Gly
NM_000216.4:c.136C>G MANE Select NP_000207.2:p.Arg46Gly
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