Canonical Allele Identifier: CA350592011
Gene: WNT10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219757889C>A (hg19) chr2:g.218893167C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893167C>A , CM000664.2:g.218893167C>A GRCh38
NC_000002.11:g.219757889C>A , CM000664.1:g.219757889C>A GRCh37
NC_000002.10:g.219466133C>A NCBI36
NG_012179.1:g.17635C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000258411.8:c.1150C>A MANE Select ENSP00000258411.3:p.Leu384Met
ENST00000258411.7:c.1150C>A ENSP00000258411.3:p.Leu384Met
NM_025216.2:c.1150C>A NP_079492.2:p.Leu384Met
XM_011511928.1:c.1099C>A XP_011510230.1:p.Leu367Met
XM_011511929.1:c.1054C>A XP_011510231.1:p.Leu352Met
XM_011511930.1:c.770C>A XP_011510232.1:p.Pro257His
XM_011511929.2:c.1054C>A XP_011510231.1:p.Leu352Met
NM_025216.3:c.1150C>A MANE Select NP_079492.2:p.Leu384Met
Search 100 bp 5'
Search 100 bp 3'