Canonical Allele Identifier: CA350618114
Gene: WNT10A HGNC NCBI

Linked Data

dbSNP Id: rs1296704490

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882187T>C , CM000664.2:g.218882187T>C GRCh38
NC_000002.11:g.219746909T>C , CM000664.1:g.219746909T>C GRCh37
NC_000002.10:g.219455153T>C NCBI36
NG_012179.1:g.6655T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.140T>C MANE Select ENSP00000258411.3:p.Leu47Pro
ENST00000258411.7:c.140T>C ENSP00000258411.3:p.Leu47Pro
ENST00000458582.1:c.27T>C
NM_025216.2:c.140T>C NP_079492.2:p.Leu47Pro
XM_011511928.1:c.89T>C XP_011510230.1:p.Leu30Pro
XM_011511929.1:c.44T>C XP_011510231.1:p.Leu15Pro
XM_011511930.1:c.140T>C XP_011510232.1:p.Leu47Pro
XM_011511929.2:c.44T>C XP_011510231.1:p.Leu15Pro
NM_025216.3:c.140T>C MANE Select NP_079492.2:p.Leu47Pro