Canonical Allele Identifier: CA412024697
Gene: ANOS1 HGNC NCBI

Linked Data

dbSNP Id: rs1246827803
gnomAD v2: X-8700055-G-T
gnomAD v4: X-8732014-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8732014G>T , CM000685.2:g.8732014G>T GRCh38
NC_000023.10:g.8700055G>T , CM000685.1:g.8700055G>T GRCh37
NC_000023.9:g.8660055G>T NCBI36
NG_007088.1:g.5173C>A
NG_007088.2:g.5173C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262648.8:c.23C>A MANE Select ENSP00000262648.3:p.Ala8Glu
ENST00000262648.7:c.23C>A ENSP00000262648.3:p.Ala8Glu
ENST00000619786.1:c.23C>A ENSP00000478734.1:p.Ala8Glu
NM_000216.2:c.23C>A NP_000207.2:p.Ala8Glu
XM_005274501.3:c.23C>A XP_005274558.1:p.Ala8Glu
NM_000216.3:c.23C>A NP_000207.2:p.Ala8Glu
XM_005274501.4:c.23C>A XP_005274558.1:p.Ala8Glu
NM_000216.4:c.23C>A MANE Select NP_000207.2:p.Ala8Glu