Canonical Allele Identifier: CA350592466

Gene: WNT10A

Linked Data

• gnomAD v4: 2-218893211-G-T
• MyVariant Identifiers: chr2:g.219757933G>T (hg19) ; chr2:g.218893211G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893211G>T , CM000664.2:g.218893211G>T	GRCh38
NC_000002.11:g.219757933G>T , CM000664.1:g.219757933G>T	GRCh37
NC_000002.10:g.219466177G>T	NCBI36
NG_012179.1:g.17679G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1194G>T MANE Select	ENSP00000258411.3:p.Trp398Cys
ENST00000258411.7:c.1194G>T	ENSP00000258411.3:p.Trp398Cys
NM_025216.2:c.1194G>T	NP_079492.2:p.Trp398Cys
XM_011511928.1:c.1143G>T	XP_011510230.1:p.Trp381Cys
XM_011511929.1:c.1098G>T	XP_011510231.1:p.Trp366Cys
XM_011511930.1:c.814G>T	XP_011510232.1:p.Val272Leu
XM_011511929.2:c.1098G>T	XP_011510231.1:p.Trp366Cys
NM_025216.3:c.1194G>T MANE Select	NP_079492.2:p.Trp398Cys