Canonical Allele Identifier: CA10343862
Gene: ANOS1 HGNC NCBI

Linked Data

dbSNP Id: rs749342096
gnomAD v2: X-8699953-C-T
gnomAD v3: X-8731912-C-T
gnomAD v4: X-8731912-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8731912C>T , CM000685.2:g.8731912C>T GRCh38
NC_000023.10:g.8699953C>T , CM000685.1:g.8699953C>T GRCh37
NC_000023.9:g.8659953C>T NCBI36
NG_007088.1:g.5275G>A
NG_007088.2:g.5275G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262648.8:c.125G>A MANE Select ENSP00000262648.3:p.Gly42Glu
ENST00000262648.7:c.125G>A ENSP00000262648.3:p.Gly42Glu
ENST00000619786.1:c.123G>A ENSP00000478734.1:p.Arg41=
NM_000216.2:c.125G>A NP_000207.2:p.Gly42Glu
XM_005274501.3:c.125G>A XP_005274558.1:p.Gly42Glu
NM_000216.3:c.125G>A NP_000207.2:p.Gly42Glu
XM_005274501.4:c.125G>A XP_005274558.1:p.Gly42Glu
NM_000216.4:c.125G>A MANE Select NP_000207.2:p.Gly42Glu