Canonical Allele Identifier: CA350592528
Gene: WNT10A HGNC NCBI

Linked Data

gnomAD v4: 2-218893218-T-A
MyVariant Identifiers: chr2:g.219757940T>A (hg19) chr2:g.218893218T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893218T>A , CM000664.2:g.218893218T>A GRCh38
NC_000002.11:g.219757940T>A , CM000664.1:g.219757940T>A GRCh37
NC_000002.10:g.219466184T>A NCBI36
NG_012179.1:g.17686T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1201T>A MANE Select ENSP00000258411.3:p.Phe401Ile
ENST00000258411.7:c.1201T>A ENSP00000258411.3:p.Phe401Ile
NM_025216.2:c.1201T>A NP_079492.2:p.Phe401Ile
XM_011511928.1:c.1150T>A XP_011510230.1:p.Phe384Ile
XM_011511929.1:c.1105T>A XP_011510231.1:p.Phe369Ile
XM_011511930.1:c.821T>A XP_011510232.1:p.Phe274Tyr
XM_011511929.2:c.1105T>A XP_011510231.1:p.Phe369Ile
NM_025216.3:c.1201T>A MANE Select NP_079492.2:p.Phe401Ile
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