Canonical Allele Identifier: CA2663174690
Gene: WNT10A HGNC NCBI

Linked Data

gnomAD v4: 2-218893395-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893395C>A , CM000664.2:g.218893395C>A GRCh38
NC_000002.11:g.219758117C>A , CM000664.1:g.219758117C>A GRCh37
NC_000002.10:g.219466361C>A NCBI36
NG_012179.1:g.17863C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.*124C>A MANE Select ENSP00000258411.3:n.*124C>A
ENST00000258411.7:c.*124C>A ENSP00000258411.3:n.*124C>A
ENST00000489887.1:n.47+128C>A
NM_025216.2:c.*124C>A NP_079492.2:n.*124C>A
XM_011511928.1:c.*124C>A XP_011510230.1:n.*124C>A
XM_011511929.1:c.*124C>A XP_011510231.1:n.*124C>A
XM_011511930.1:c.*98C>A XP_011510232.1:n.*98C>A
XM_011511929.2:c.*124C>A XP_011510231.1:n.*124C>A
NM_025216.3:c.*124C>A MANE Select NP_079492.2:n.*124C>A
Search 100 bp 5'
Search 100 bp 3'