Canonical Allele Identifier: CA350592831

Gene: WNT10A

Linked Data

• gnomAD v4: 2-218893259-C-A
• MyVariant Identifiers: chr2:g.219757981C>A (hg19) ; chr2:g.218893259C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893259C>A , CM000664.2:g.218893259C>A	GRCh38
NC_000002.11:g.219757981C>A , CM000664.1:g.219757981C>A	GRCh37
NC_000002.10:g.219466225C>A	NCBI36
NG_012179.1:g.17727C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1242C>A MANE Select	ENSP00000258411.3:p.Ser414Arg
ENST00000258411.7:c.1242C>A	ENSP00000258411.3:p.Ser414Arg
ENST00000489887.1:n.39C>A
NM_025216.2:c.1242C>A	NP_079492.2:p.Ser414Arg
XM_011511928.1:c.1191C>A	XP_011510230.1:p.Ser397Arg
XM_011511929.1:c.1146C>A	XP_011510231.1:p.Ser382Arg
XM_011511930.1:c.862C>A	XP_011510232.1:p.Arg288Ser
XM_011511929.2:c.1146C>A	XP_011510231.1:p.Ser382Arg
NM_025216.3:c.1242C>A MANE Select	NP_079492.2:p.Ser414Arg