Canonical Allele Identifier: CA2414666192
Gene: ANOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8731801A= , CM000685.2:g.8731801A= GRCh38
NC_000023.10:g.8699842A= , CM000685.1:g.8699842A= GRCh37
NC_000023.9:g.8659842A= NCBI36
NG_007088.1:g.5386T=
NG_007088.2:g.5386T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262648.8:c.207+29T= MANE Select ENSP00000262648.3:n.207+29T=
ENST00000262648.7:c.207+29T= ENSP00000262648.3:n.207+29T=
ENST00000619786.1:c.204+29T= ENSP00000478734.1:n.204+29T=
NM_000216.2:c.207+29T= NP_000207.2:n.207+29T=
XM_005274501.3:c.207+29T= XP_005274558.1:n.207+29T=
NM_000216.3:c.207+29T= NP_000207.2:n.207+29T=
XM_005274501.4:c.207+29T= XP_005274558.1:n.207+29T=
NM_000216.4:c.207+29T= MANE Select NP_000207.2:n.207+29T=