Canonical Allele Identifier: CA350592533
Gene: WNT10A HGNC NCBI

Linked Data

gnomAD v4: 2-218893219-T-C
MyVariant Identifiers: chr2:g.219757941T>C (hg19) chr2:g.218893219T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893219T>C , CM000664.2:g.218893219T>C GRCh38
NC_000002.11:g.219757941T>C , CM000664.1:g.219757941T>C GRCh37
NC_000002.10:g.219466185T>C NCBI36
NG_012179.1:g.17687T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1202T>C MANE Select ENSP00000258411.3:p.Phe401Ser
ENST00000258411.7:c.1202T>C ENSP00000258411.3:p.Phe401Ser
NM_025216.2:c.1202T>C NP_079492.2:p.Phe401Ser
XM_011511928.1:c.1151T>C XP_011510230.1:p.Phe384Ser
XM_011511929.1:c.1106T>C XP_011510231.1:p.Phe369Ser
XM_011511930.1:c.822T>C XP_011510232.1:p.Phe274=
XM_011511929.2:c.1106T>C XP_011510231.1:p.Phe369Ser
NM_025216.3:c.1202T>C MANE Select NP_079492.2:p.Phe401Ser
Search 100 bp 5'
Search 100 bp 3'