Canonical Allele Identifier: CA2414666219
Gene: ANOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8731867T= , CM000685.2:g.8731867T= GRCh38
NC_000023.10:g.8699908T= , CM000685.1:g.8699908T= GRCh37
NC_000023.9:g.8659908T= NCBI36
NG_007088.1:g.5320A=
NG_007088.2:g.5320A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262648.8:c.170A= MANE Select ENSP00000262648.3:p.Gln57=
ENST00000262648.7:c.170A= ENSP00000262648.3:p.Gln57=
ENST00000619786.1:c.167A= ENSP00000478734.1:p.Gln56=
NM_000216.2:c.170A= NP_000207.2:p.Gln57=
XM_005274501.3:c.170A= XP_005274558.1:p.Gln57=
NM_000216.3:c.170A= NP_000207.2:p.Gln57=
XM_005274501.4:c.170A= XP_005274558.1:p.Gln57=
NM_000216.4:c.170A= MANE Select NP_000207.2:p.Gln57=