Canonical Allele Identifier: CA2414618762
Gene: ANOS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8587721T= , CM000685.2:g.8587721T= GRCh38
NC_000023.10:g.8555762T= , CM000685.1:g.8555762T= GRCh37
NC_000023.9:g.8515762T= NCBI36
NG_007088.1:g.149466A=
NG_007088.2:g.149466A=

Transcript Alleles

HGVS Amino-acid change
ENST00000262648.8:c.726+73A= MANE Select ENSP00000262648.3:n.726+73A=
ENST00000262648.7:c.726+73A= ENSP00000262648.3:n.726+73A=
ENST00000619786.1:c.723+73A= ENSP00000478734.1:n.723+73A=
NM_000216.2:c.726+73A= NP_000207.2:n.726+73A=
XM_005274501.3:c.726+73A= XP_005274558.1:n.726+73A=
NM_000216.3:c.726+73A= NP_000207.2:n.726+73A=
XM_005274501.4:c.726+73A= XP_005274558.1:n.726+73A=
NM_000216.4:c.726+73A= MANE Select NP_000207.2:n.726+73A=
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