Canonical Allele Identifier: CA2414666217
Gene: ANOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8731862T= , CM000685.2:g.8731862T= GRCh38
NC_000023.10:g.8699903T= , CM000685.1:g.8699903T= GRCh37
NC_000023.9:g.8659903T= NCBI36
NG_007088.1:g.5325A=
NG_007088.2:g.5325A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262648.8:c.175A= MANE Select ENSP00000262648.3:p.Thr59=
ENST00000262648.7:c.175A= ENSP00000262648.3:p.Thr59=
ENST00000619786.1:c.172A= ENSP00000478734.1:p.Thr58=
NM_000216.2:c.175A= NP_000207.2:p.Thr59=
XM_005274501.3:c.175A= XP_005274558.1:p.Thr59=
NM_000216.3:c.175A= NP_000207.2:p.Thr59=
XM_005274501.4:c.175A= XP_005274558.1:p.Thr59=
NM_000216.4:c.175A= MANE Select NP_000207.2:p.Thr59=