Canonical Allele Identifier: CA412023843
Gene: ANOS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.8555851C>T (hg19) chrX:g.8587810C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8587810C>T , CM000685.2:g.8587810C>T GRCh38
NC_000023.10:g.8555851C>T , CM000685.1:g.8555851C>T GRCh37
NC_000023.9:g.8515851C>T NCBI36
NG_007088.1:g.149377G>A
NG_007088.2:g.149377G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262648.8:c.710G>A MANE Select ENSP00000262648.3:p.Trp237Ter
ENST00000262648.7:c.710G>A ENSP00000262648.3:p.Trp237Ter
ENST00000619786.1:c.707G>A ENSP00000478734.1:p.Trp236Ter
NM_000216.2:c.710G>A NP_000207.2:p.Trp237Ter
XM_005274501.3:c.710G>A XP_005274558.1:p.Trp237Ter
NM_000216.3:c.710G>A NP_000207.2:p.Trp237Ter
XM_005274501.4:c.710G>A XP_005274558.1:p.Trp237Ter
NM_000216.4:c.710G>A MANE Select NP_000207.2:p.Trp237Ter
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