Canonical Allele Identifier: CA350587027
Gene: WNT10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219754988T>A (hg19) chr2:g.218890266T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218890266T>A , CM000664.2:g.218890266T>A GRCh38
NC_000002.11:g.219754988T>A , CM000664.1:g.219754988T>A GRCh37
NC_000002.10:g.219463232T>A NCBI36
NG_012179.1:g.14734T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000258411.8:c.659T>A MANE Select ENSP00000258411.3:p.Phe220Tyr
ENST00000258411.7:c.659T>A ENSP00000258411.3:p.Phe220Tyr
ENST00000458582.1:c.264-2508T>A
NM_025216.2:c.659T>A NP_079492.2:p.Phe220Tyr
XM_011511928.1:c.608T>A XP_011510230.1:p.Phe203Tyr
XM_011511929.1:c.563T>A XP_011510231.1:p.Phe188Tyr
XM_011511930.1:c.377-2508T>A XP_011510232.1:n.377-2508T>A
XM_011511929.2:c.563T>A XP_011510231.1:p.Phe188Tyr
NM_025216.3:c.659T>A MANE Select NP_079492.2:p.Phe220Tyr
Search 100 bp 5'
Search 100 bp 3'