Canonical Allele Identifier: CA350587035

Gene: WNT10A

Linked Data

• MyVariant Identifiers: chr2:g.219754988T>G (hg19) ; chr2:g.218890266T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218890266T>G , CM000664.2:g.218890266T>G	GRCh38
NC_000002.11:g.219754988T>G , CM000664.1:g.219754988T>G	GRCh37
NC_000002.10:g.219463232T>G	NCBI36
NG_012179.1:g.14734T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000258411.8:c.659T>G MANE Select	ENSP00000258411.3:p.Phe220Cys
ENST00000258411.7:c.659T>G	ENSP00000258411.3:p.Phe220Cys
ENST00000458582.1:c.264-2508T>G
NM_025216.2:c.659T>G	NP_079492.2:p.Phe220Cys
XM_011511928.1:c.608T>G	XP_011510230.1:p.Phe203Cys
XM_011511929.1:c.563T>G	XP_011510231.1:p.Phe188Cys
XM_011511930.1:c.377-2508T>G	XP_011510232.1:n.377-2508T>G
XM_011511929.2:c.563T>G	XP_011510231.1:p.Phe188Cys
NM_025216.3:c.659T>G MANE Select	NP_079492.2:p.Phe220Cys