Canonical Allele Identifier: CA350592208

Gene: WNT10A

Linked Data

• gnomAD v4: 2-218893188-C-T
• MyVariant Identifiers: chr2:g.219757910C>T (hg19) ; chr2:g.218893188C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893188C>T , CM000664.2:g.218893188C>T	GRCh38
NC_000002.11:g.219757910C>T , CM000664.1:g.219757910C>T	GRCh37
NC_000002.10:g.219466154C>T	NCBI36
NG_012179.1:g.17656C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1171C>T MANE Select	ENSP00000258411.3:p.Arg391Cys
ENST00000258411.7:c.1171C>T	ENSP00000258411.3:p.Arg391Cys
NM_025216.2:c.1171C>T	NP_079492.2:p.Arg391Cys
XM_011511928.1:c.1120C>T	XP_011510230.1:p.Arg374Cys
XM_011511929.1:c.1075C>T	XP_011510231.1:p.Arg359Cys
XM_011511930.1:c.791C>T	XP_011510232.1:p.Ala264Val
XM_011511929.2:c.1075C>T	XP_011510231.1:p.Arg359Cys
NM_025216.3:c.1171C>T MANE Select	NP_079492.2:p.Arg391Cys