Canonical Allele Identifier: CA350618168
Gene: WNT10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219746920C>A (hg19) chr2:g.218882198C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882198C>A , CM000664.2:g.218882198C>A GRCh38
NC_000002.11:g.219746920C>A , CM000664.1:g.219746920C>A GRCh37
NC_000002.10:g.219455164C>A NCBI36
NG_012179.1:g.6666C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.151C>A MANE Select ENSP00000258411.3:p.Pro51Thr
ENST00000258411.7:c.151C>A ENSP00000258411.3:p.Pro51Thr
ENST00000458582.1:c.38C>A
NM_025216.2:c.151C>A NP_079492.2:p.Pro51Thr
XM_011511928.1:c.100C>A XP_011510230.1:p.Pro34Thr
XM_011511929.1:c.55C>A XP_011510231.1:p.Pro19Thr
XM_011511930.1:c.151C>A XP_011510232.1:p.Pro51Thr
XM_011511929.2:c.55C>A XP_011510231.1:p.Pro19Thr
NM_025216.3:c.151C>A MANE Select NP_079492.2:p.Pro51Thr
Search 100 bp 5'
Search 100 bp 3'