Canonical Allele Identifier: CA2414618792
Gene: ANOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8587813T= , CM000685.2:g.8587813T= GRCh38
NC_000023.10:g.8555854T= , CM000685.1:g.8555854T= GRCh37
NC_000023.9:g.8515854T= NCBI36
NG_007088.1:g.149374A=
NG_007088.2:g.149374A=

Transcript Alleles

HGVS Amino-acid change
ENST00000262648.8:c.707A= MANE Select ENSP00000262648.3:p.His236=
ENST00000262648.7:c.707A= ENSP00000262648.3:p.His236=
ENST00000619786.1:c.704A= ENSP00000478734.1:p.His235=
NM_000216.2:c.707A= NP_000207.2:p.His236=
XM_005274501.3:c.707A= XP_005274558.1:p.His236=
NM_000216.3:c.707A= NP_000207.2:p.His236=
XM_005274501.4:c.707A= XP_005274558.1:p.His236=
NM_000216.4:c.707A= MANE Select NP_000207.2:p.His236=