Canonical Allele Identifier: CA431416479

Gene: WNT10A

Linked Data

• MyVariant Identifiers: chr2:g.219747006T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882284T>G , CM000664.2:g.218882284T>G	GRCh38
NC_000002.11:g.219747006T>G , CM000664.1:g.219747006T>G	GRCh37
NC_000002.10:g.219455250T>G	NCBI36
NG_012179.1:g.6752T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.237T>G MANE Select	ENSP00000258411.3:p.Pro79=
ENST00000258411.7:c.237T>G	ENSP00000258411.3:p.Pro79=
ENST00000458582.1:c.124T>G
NM_025216.2:c.237T>G	NP_079492.2:p.Pro79=
XM_011511928.1:c.186T>G	XP_011510230.1:p.Pro62=
XM_011511929.1:c.141T>G	XP_011510231.1:p.Pro47=
XM_011511930.1:c.237T>G	XP_011510232.1:p.Pro79=
XM_011511929.2:c.141T>G	XP_011510231.1:p.Pro47=
NM_025216.3:c.237T>G MANE Select	NP_079492.2:p.Pro79=