Canonical Allele Identifier: CA412024422
Gene: ANOS1 HGNC NCBI

Linked Data

gnomAD v4: X-8731906-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8731906A>C , CM000685.2:g.8731906A>C GRCh38
NC_000023.10:g.8699947A>C , CM000685.1:g.8699947A>C GRCh37
NC_000023.9:g.8659947A>C NCBI36
NG_007088.1:g.5281T>G
NG_007088.2:g.5281T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262648.8:c.131T>G MANE Select ENSP00000262648.3:p.Val44Gly
ENST00000262648.7:c.131T>G ENSP00000262648.3:p.Val44Gly
ENST00000619786.1:c.129T>G ENSP00000478734.1:p.Arg43=
NM_000216.2:c.131T>G NP_000207.2:p.Val44Gly
XM_005274501.3:c.131T>G XP_005274558.1:p.Val44Gly
NM_000216.3:c.131T>G NP_000207.2:p.Val44Gly
XM_005274501.4:c.131T>G XP_005274558.1:p.Val44Gly
NM_000216.4:c.131T>G MANE Select NP_000207.2:p.Val44Gly