Canonical Allele Identifier: CA350592093
Gene: WNT10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219757898A>G (hg19) chr2:g.218893176A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893176A>G , CM000664.2:g.218893176A>G GRCh38
NC_000002.11:g.219757898A>G , CM000664.1:g.219757898A>G GRCh37
NC_000002.10:g.219466142A>G NCBI36
NG_012179.1:g.17644A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1159A>G MANE Select ENSP00000258411.3:p.Thr387Ala
ENST00000258411.7:c.1159A>G ENSP00000258411.3:p.Thr387Ala
NM_025216.2:c.1159A>G NP_079492.2:p.Thr387Ala
XM_011511928.1:c.1108A>G XP_011510230.1:p.Thr370Ala
XM_011511929.1:c.1063A>G XP_011510231.1:p.Thr355Ala
XM_011511930.1:c.779A>G XP_011510232.1:p.Asp260Gly
XM_011511929.2:c.1063A>G XP_011510231.1:p.Thr355Ala
NM_025216.3:c.1159A>G MANE Select NP_079492.2:p.Thr387Ala
Search 100 bp 5'
Search 100 bp 3'