Canonical Allele Identifier: CA2414666259
Gene: ANOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8731947A= , CM000685.2:g.8731947A= GRCh38
NC_000023.10:g.8699988A= , CM000685.1:g.8699988A= GRCh37
NC_000023.9:g.8659988A= NCBI36
NG_007088.1:g.5240T=
NG_007088.2:g.5240T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262648.8:c.90T= MANE Select ENSP00000262648.3:p.Ala30=
ENST00000262648.7:c.90T= ENSP00000262648.3:p.Ala30=
ENST00000619786.1:c.89T= ENSP00000478734.1:p.Leu30=
NM_000216.2:c.90T= NP_000207.2:p.Ala30=
XM_005274501.3:c.90T= XP_005274558.1:p.Ala30=
NM_000216.3:c.90T= NP_000207.2:p.Ala30=
XM_005274501.4:c.90T= XP_005274558.1:p.Ala30=
NM_000216.4:c.90T= MANE Select NP_000207.2:p.Ala30=