Canonical Allele Identifier: CA350618675
Gene: WNT10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219747010G>A (hg19) chr2:g.218882288G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882288G>A , CM000664.2:g.218882288G>A GRCh38
NC_000002.11:g.219747010G>A , CM000664.1:g.219747010G>A GRCh37
NC_000002.10:g.219455254G>A NCBI36
NG_012179.1:g.6756G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.241G>A MANE Select ENSP00000258411.3:p.Val81Met
ENST00000258411.7:c.241G>A ENSP00000258411.3:p.Val81Met
ENST00000458582.1:c.128G>A
NM_025216.2:c.241G>A NP_079492.2:p.Val81Met
XM_011511928.1:c.190G>A XP_011510230.1:p.Val64Met
XM_011511929.1:c.145G>A XP_011510231.1:p.Val49Met
XM_011511930.1:c.241G>A XP_011510232.1:p.Val81Met
XM_011511929.2:c.145G>A XP_011510231.1:p.Val49Met
NM_025216.3:c.241G>A MANE Select NP_079492.2:p.Val81Met
Search 100 bp 5'
Search 100 bp 3'