Canonical Allele Identifier: CA350618276
Gene: WNT10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219746938G>A (hg19) chr2:g.218882216G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882216G>A , CM000664.2:g.218882216G>A GRCh38
NC_000002.11:g.219746938G>A , CM000664.1:g.219746938G>A GRCh37
NC_000002.10:g.219455182G>A NCBI36
NG_012179.1:g.6684G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.169G>A MANE Select ENSP00000258411.3:p.Ala57Thr
ENST00000258411.7:c.169G>A ENSP00000258411.3:p.Ala57Thr
ENST00000458582.1:c.56G>A
NM_025216.2:c.169G>A NP_079492.2:p.Ala57Thr
XM_011511928.1:c.118G>A XP_011510230.1:p.Ala40Thr
XM_011511929.1:c.73G>A XP_011510231.1:p.Ala25Thr
XM_011511930.1:c.169G>A XP_011510232.1:p.Ala57Thr
XM_011511929.2:c.73G>A XP_011510231.1:p.Ala25Thr
NM_025216.3:c.169G>A MANE Select NP_079492.2:p.Ala57Thr
Search 100 bp 5'
Search 100 bp 3'