Canonical Allele Identifier: CA412024279
Gene: ANOS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.8699885A>C (hg19) chrX:g.8731844A>C (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000262648.8:c.193T>G MANE Select ENSP00000262648.3:p.Phe65Val
ENST00000262648.7:c.193T>G ENSP00000262648.3:p.Phe65Val
ENST00000619786.1:c.190T>G ENSP00000478734.1:p.Phe64Val
NM_000216.2:c.193T>G NP_000207.2:p.Phe65Val
XM_005274501.3:c.193T>G XP_005274558.1:p.Phe65Val
NM_000216.3:c.193T>G NP_000207.2:p.Phe65Val
XM_005274501.4:c.193T>G XP_005274558.1:p.Phe65Val
NM_000216.4:c.193T>G MANE Select NP_000207.2:p.Phe65Val
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