Canonical Allele Identifier: CA350618080
Gene: WNT10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219746903T>G (hg19) chr2:g.218882181T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882181T>G , CM000664.2:g.218882181T>G GRCh38
NC_000002.11:g.219746903T>G , CM000664.1:g.219746903T>G GRCh37
NC_000002.10:g.219455147T>G NCBI36
NG_012179.1:g.6649T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.134T>G MANE Select ENSP00000258411.3:p.Leu45Arg
ENST00000258411.7:c.134T>G ENSP00000258411.3:p.Leu45Arg
ENST00000458582.1:c.21T>G
NM_025216.2:c.134T>G NP_079492.2:p.Leu45Arg
XM_011511928.1:c.83T>G XP_011510230.1:p.Leu28Arg
XM_011511929.1:c.38T>G XP_011510231.1:p.Leu13Arg
XM_011511930.1:c.134T>G XP_011510232.1:p.Leu45Arg
XM_011511929.2:c.38T>G XP_011510231.1:p.Leu13Arg
NM_025216.3:c.134T>G MANE Select NP_079492.2:p.Leu45Arg
Search 100 bp 5'
Search 100 bp 3'