Canonical Allele Identifier: CA2113845
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1128951
ClinVar RCV Id: RCV001461911
dbSNP Id: rs761730775

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882197C>T , CM000664.2:g.218882197C>T GRCh38
NC_000002.11:g.219746919C>T , CM000664.1:g.219746919C>T GRCh37
NC_000002.10:g.219455163C>T NCBI36
NG_012179.1:g.6665C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.150C>T MANE Select ENSP00000258411.3:p.Pro50=
ENST00000258411.7:c.150C>T ENSP00000258411.3:p.Pro50=
ENST00000458582.1:c.37C>T
NM_025216.2:c.150C>T NP_079492.2:p.Pro50=
XM_011511928.1:c.99C>T XP_011510230.1:p.Pro33=
XM_011511929.1:c.54C>T XP_011510231.1:p.Pro18=
XM_011511930.1:c.150C>T XP_011510232.1:p.Pro50=
XM_011511929.2:c.54C>T XP_011510231.1:p.Pro18=
NM_025216.3:c.150C>T MANE Select NP_079492.2:p.Pro50=