Canonical Allele Identifier: CA2414666153
Gene: ANOS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8731711G= , CM000685.2:g.8731711G= GRCh38
NC_000023.10:g.8699752G= , CM000685.1:g.8699752G= GRCh37
NC_000023.9:g.8659752G= NCBI36
NG_007088.1:g.5476C=
NG_007088.2:g.5476C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262648.8:c.207+119C= MANE Select ENSP00000262648.3:n.207+119C=
ENST00000262648.7:c.207+119C= ENSP00000262648.3:n.207+119C=
ENST00000619786.1:c.204+119C= ENSP00000478734.1:n.204+119C=
NM_000216.2:c.207+119C= NP_000207.2:n.207+119C=
XM_005274501.3:c.207+119C= XP_005274558.1:n.207+119C=
NM_000216.3:c.207+119C= NP_000207.2:n.207+119C=
XM_005274501.4:c.207+119C= XP_005274558.1:n.207+119C=
NM_000216.4:c.207+119C= MANE Select NP_000207.2:n.207+119C=
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