Canonical Allele Identifier: CA350592384
Gene: WNT10A HGNC NCBI

Linked Data

gnomAD v4: 2-218893205-C-A
MyVariant Identifiers: chr2:g.219757927C>A (hg19) chr2:g.218893205C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893205C>A , CM000664.2:g.218893205C>A GRCh38
NC_000002.11:g.219757927C>A , CM000664.1:g.219757927C>A GRCh37
NC_000002.10:g.219466171C>A NCBI36
NG_012179.1:g.17673C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1188C>A MANE Select ENSP00000258411.3:p.Phe396Leu
ENST00000258411.7:c.1188C>A ENSP00000258411.3:p.Phe396Leu
NM_025216.2:c.1188C>A NP_079492.2:p.Phe396Leu
XM_011511928.1:c.1137C>A XP_011510230.1:p.Phe379Leu
XM_011511929.1:c.1092C>A XP_011510231.1:p.Phe364Leu
XM_011511930.1:c.808C>A XP_011510232.1:p.Pro270Thr
XM_011511929.2:c.1092C>A XP_011510231.1:p.Phe364Leu
NM_025216.3:c.1188C>A MANE Select NP_079492.2:p.Phe396Leu
Search 100 bp 5'
Search 100 bp 3'