Canonical Allele Identifier: CA431416446
Gene: WNT10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219746958A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882236A>C , CM000664.2:g.218882236A>C GRCh38
NC_000002.11:g.219746958A>C , CM000664.1:g.219746958A>C GRCh37
NC_000002.10:g.219455202A>C NCBI36
NG_012179.1:g.6704A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.189A>C MANE Select ENSP00000258411.3:p.Thr63=
ENST00000258411.7:c.189A>C ENSP00000258411.3:p.Thr63=
ENST00000458582.1:c.76A>C
NM_025216.2:c.189A>C NP_079492.2:p.Thr63=
XM_011511928.1:c.138A>C XP_011510230.1:p.Thr46=
XM_011511929.1:c.93A>C XP_011510231.1:p.Thr31=
XM_011511930.1:c.189A>C XP_011510232.1:p.Thr63=
XM_011511929.2:c.93A>C XP_011510231.1:p.Thr31=
NM_025216.3:c.189A>C MANE Select NP_079492.2:p.Thr63=
Search 100 bp 5'
Search 100 bp 3'