Canonical Allele Identifier: CA431417544
Gene: WNT10A HGNC NCBI

Linked Data

gnomAD v4: 2-218893169-G-A
MyVariant Identifiers: chr2:g.219757891G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893169G>A , CM000664.2:g.218893169G>A GRCh38
NC_000002.11:g.219757891G>A , CM000664.1:g.219757891G>A GRCh37
NC_000002.10:g.219466135G>A NCBI36
NG_012179.1:g.17637G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000258411.8:c.1152G>A MANE Select ENSP00000258411.3:p.Leu384=
ENST00000258411.7:c.1152G>A ENSP00000258411.3:p.Leu384=
NM_025216.2:c.1152G>A NP_079492.2:p.Leu384=
XM_011511928.1:c.1101G>A XP_011510230.1:p.Leu367=
XM_011511929.1:c.1056G>A XP_011510231.1:p.Leu352=
XM_011511930.1:c.772G>A XP_011510232.1:p.Ala258Thr
XM_011511929.2:c.1056G>A XP_011510231.1:p.Leu352=
NM_025216.3:c.1152G>A MANE Select NP_079492.2:p.Leu384=
Search 100 bp 5'
Search 100 bp 3'