Canonical Allele Identifier: CA350592551
Gene: WNT10A HGNC NCBI

Linked Data

gnomAD v4: 2-218893222-T-C
MyVariant Identifiers: chr2:g.219757944T>C (hg19) chr2:g.218893222T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893222T>C , CM000664.2:g.218893222T>C GRCh38
NC_000002.11:g.219757944T>C , CM000664.1:g.219757944T>C GRCh37
NC_000002.10:g.219466188T>C NCBI36
NG_012179.1:g.17690T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1205T>C MANE Select ENSP00000258411.3:p.Val402Ala
ENST00000258411.7:c.1205T>C ENSP00000258411.3:p.Val402Ala
ENST00000489887.1:n.2T>C
NM_025216.2:c.1205T>C NP_079492.2:p.Val402Ala
XM_011511928.1:c.1154T>C XP_011510230.1:p.Val385Ala
XM_011511929.1:c.1109T>C XP_011510231.1:p.Val370Ala
XM_011511930.1:c.825T>C XP_011510232.1:p.Arg275=
XM_011511929.2:c.1109T>C XP_011510231.1:p.Val370Ala
NM_025216.3:c.1205T>C MANE Select NP_079492.2:p.Val402Ala
Search 100 bp 5'
Search 100 bp 3'