Canonical Allele Identifier: CA350587022

Gene: WNT10A

Linked Data

• MyVariant Identifiers: chr2:g.219754987T>G (hg19) ; chr2:g.218890265T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218890265T>G , CM000664.2:g.218890265T>G	GRCh38
NC_000002.11:g.219754987T>G , CM000664.1:g.219754987T>G	GRCh37
NC_000002.10:g.219463231T>G	NCBI36
NG_012179.1:g.14733T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000258411.8:c.658T>G MANE Select	ENSP00000258411.3:p.Phe220Val
ENST00000258411.7:c.658T>G	ENSP00000258411.3:p.Phe220Val
ENST00000458582.1:c.264-2509T>G
NM_025216.2:c.658T>G	NP_079492.2:p.Phe220Val
XM_011511928.1:c.607T>G	XP_011510230.1:p.Phe203Val
XM_011511929.1:c.562T>G	XP_011510231.1:p.Phe188Val
XM_011511930.1:c.377-2509T>G	XP_011510232.1:n.377-2509T>G
XM_011511929.2:c.562T>G	XP_011510231.1:p.Phe188Val
NM_025216.3:c.658T>G MANE Select	NP_079492.2:p.Phe220Val