Canonical Allele Identifier: CA350592462

Gene: WNT10A

Linked Data

• gnomAD v4: 2-218893210-G-T
• MyVariant Identifiers: chr2:g.219757932G>T (hg19) ; chr2:g.218893210G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893210G>T , CM000664.2:g.218893210G>T	GRCh38
NC_000002.11:g.219757932G>T , CM000664.1:g.219757932G>T	GRCh37
NC_000002.10:g.219466176G>T	NCBI36
NG_012179.1:g.17678G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1193G>T MANE Select	ENSP00000258411.3:p.Trp398Leu
ENST00000258411.7:c.1193G>T	ENSP00000258411.3:p.Trp398Leu
NM_025216.2:c.1193G>T	NP_079492.2:p.Trp398Leu
XM_011511928.1:c.1142G>T	XP_011510230.1:p.Trp381Leu
XM_011511929.1:c.1097G>T	XP_011510231.1:p.Trp366Leu
XM_011511930.1:c.813G>T	XP_011510232.1:p.Leu271=
XM_011511929.2:c.1097G>T	XP_011510231.1:p.Trp366Leu
NM_025216.3:c.1193G>T MANE Select	NP_079492.2:p.Trp398Leu