Canonical Allele Identifier: CA515172554
Gene: ANOS1 HGNC NCBI

Linked Data

gnomAD v4: X-8732028-G-T
MyVariant Identifiers: chrX:g.8700069G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8732028G>T , CM000685.2:g.8732028G>T GRCh38
NC_000023.10:g.8700069G>T , CM000685.1:g.8700069G>T GRCh37
NC_000023.9:g.8660069G>T NCBI36
NG_007088.1:g.5159C>A
NG_007088.2:g.5159C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262648.8:c.9C>A MANE Select ENSP00000262648.3:p.Pro3=
ENST00000262648.7:c.9C>A ENSP00000262648.3:p.Pro3=
ENST00000619786.1:c.9C>A ENSP00000478734.1:p.Pro3=
NM_000216.2:c.9C>A NP_000207.2:p.Pro3=
XM_005274501.3:c.9C>A XP_005274558.1:p.Pro3=
NM_000216.3:c.9C>A NP_000207.2:p.Pro3=
XM_005274501.4:c.9C>A XP_005274558.1:p.Pro3=
NM_000216.4:c.9C>A MANE Select NP_000207.2:p.Pro3=