Canonical Allele Identifier: CA2414666131
Gene: ANOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8731649G= , CM000685.2:g.8731649G= GRCh38
NC_000023.10:g.8699690G= , CM000685.1:g.8699690G= GRCh37
NC_000023.9:g.8659690G= NCBI36
NG_007088.1:g.5538C=
NG_007088.2:g.5538C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262648.8:c.207+181C= MANE Select ENSP00000262648.3:n.207+181C=
ENST00000262648.7:c.207+181C= ENSP00000262648.3:n.207+181C=
ENST00000619786.1:c.204+181C= ENSP00000478734.1:n.204+181C=
NM_000216.2:c.207+181C= NP_000207.2:n.207+181C=
XM_005274501.3:c.207+181C= XP_005274558.1:n.207+181C=
NM_000216.3:c.207+181C= NP_000207.2:n.207+181C=
XM_005274501.4:c.207+181C= XP_005274558.1:n.207+181C=
NM_000216.4:c.207+181C= MANE Select NP_000207.2:n.207+181C=