Canonical Allele Identifier: CA412024626
Gene: ANOS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8731979T>G , CM000685.2:g.8731979T>G GRCh38
NC_000023.10:g.8700020T>G , CM000685.1:g.8700020T>G GRCh37
NC_000023.9:g.8660020T>G NCBI36
NG_007088.1:g.5208A>C
NG_007088.2:g.5208A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262648.8:c.58A>C MANE Select ENSP00000262648.3:p.Ser20Arg
ENST00000262648.7:c.58A>C ENSP00000262648.3:p.Ser20Arg
ENST00000619786.1:c.58A>C ENSP00000478734.1:p.Ser20Arg
NM_000216.2:c.58A>C NP_000207.2:p.Ser20Arg
XM_005274501.3:c.58A>C XP_005274558.1:p.Ser20Arg
NM_000216.3:c.58A>C NP_000207.2:p.Ser20Arg
XM_005274501.4:c.58A>C XP_005274558.1:p.Ser20Arg
NM_000216.4:c.58A>C MANE Select NP_000207.2:p.Ser20Arg