Canonical Allele Identifier: CA350592730

Gene: WNT10A

Linked Data

• gnomAD v4: 2-218893240-G-T
• MyVariant Identifiers: chr2:g.219757962G>T (hg19) ; chr2:g.218893240G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893240G>T , CM000664.2:g.218893240G>T	GRCh38
NC_000002.11:g.219757962G>T , CM000664.1:g.219757962G>T	GRCh37
NC_000002.10:g.219466206G>T	NCBI36
NG_012179.1:g.17708G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1223G>T MANE Select	ENSP00000258411.3:p.Arg408Leu
ENST00000258411.7:c.1223G>T	ENSP00000258411.3:p.Arg408Leu
ENST00000489887.1:n.20G>T
NM_025216.2:c.1223G>T	NP_079492.2:p.Arg408Leu
XM_011511928.1:c.1172G>T	XP_011510230.1:p.Arg391Leu
XM_011511929.1:c.1127G>T	XP_011510231.1:p.Arg376Leu
XM_011511930.1:c.843G>T	XP_011510232.1:p.Pro281=
XM_011511929.2:c.1127G>T	XP_011510231.1:p.Arg376Leu
NM_025216.3:c.1223G>T MANE Select	NP_079492.2:p.Arg408Leu