Canonical Allele Identifier: CA764938315
Gene: WNT10A HGNC NCBI

Linked Data

dbSNP Id: rs1440656026

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218881859T>C , CM000664.2:g.218881859T>C GRCh38
NC_000002.11:g.219746581T>C , CM000664.1:g.219746581T>C GRCh37
NC_000002.10:g.219454825T>C NCBI36
NG_012179.1:g.6327T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.114-302T>C MANE Select ENSP00000258411.3:n.114-302T>C
ENST00000258411.7:c.114-302T>C ENSP00000258411.3:n.114-302T>C
NM_025216.2:c.114-302T>C NP_079492.2:n.114-302T>C
XM_011511928.1:c.63-302T>C XP_011510230.1:n.63-302T>C
XM_011511929.1:c.18-302T>C XP_011510231.1:n.18-302T>C
XM_011511930.1:c.114-302T>C XP_011510232.1:n.114-302T>C
XM_011511929.2:c.18-302T>C XP_011510231.1:n.18-302T>C
NM_025216.3:c.114-302T>C MANE Select NP_079492.2:n.114-302T>C