Canonical Allele Identifier: CA412024681
Gene: ANOS1 HGNC NCBI

Linked Data

gnomAD v4: X-8732006-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8732006T>A , CM000685.2:g.8732006T>A GRCh38
NC_000023.10:g.8700047T>A , CM000685.1:g.8700047T>A GRCh37
NC_000023.9:g.8660047T>A NCBI36
NG_007088.1:g.5181A>T
NG_007088.2:g.5181A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000262648.8:c.31A>T MANE Select ENSP00000262648.3:p.Thr11Ser
ENST00000262648.7:c.31A>T ENSP00000262648.3:p.Thr11Ser
ENST00000619786.1:c.31A>T ENSP00000478734.1:p.Thr11Ser
NM_000216.2:c.31A>T NP_000207.2:p.Thr11Ser
XM_005274501.3:c.31A>T XP_005274558.1:p.Thr11Ser
NM_000216.3:c.31A>T NP_000207.2:p.Thr11Ser
XM_005274501.4:c.31A>T XP_005274558.1:p.Thr11Ser
NM_000216.4:c.31A>T MANE Select NP_000207.2:p.Thr11Ser