Canonical Allele Identifier: CA350592560
Gene: WNT10A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893224G>C , CM000664.2:g.218893224G>C GRCh38
NC_000002.11:g.219757946G>C , CM000664.1:g.219757946G>C GRCh37
NC_000002.10:g.219466190G>C NCBI36
NG_012179.1:g.17692G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1207G>C MANE Select ENSP00000258411.3:p.Val403Leu
ENST00000258411.7:c.1207G>C ENSP00000258411.3:p.Val403Leu
ENST00000489887.1:n.4G>C
NM_025216.2:c.1207G>C NP_079492.2:p.Val403Leu
XM_011511928.1:c.1156G>C XP_011510230.1:p.Val386Leu
XM_011511929.1:c.1111G>C XP_011510231.1:p.Val371Leu
XM_011511930.1:c.827G>C XP_011510232.1:p.Gly276Ala
XM_011511929.2:c.1111G>C XP_011510231.1:p.Val371Leu
NM_025216.3:c.1207G>C MANE Select NP_079492.2:p.Val403Leu