Canonical Allele Identifier: CA431416403

Gene: WNT10A

Linked Data

• ClinVar Variation Id: 2074523
• ClinVar RCV Id: RCV002976272
• dbSNP Id: rs747317988
• MyVariant Identifiers: chr2:g.219746901T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882179T>A , CM000664.2:g.218882179T>A	GRCh38
NC_000002.11:g.219746901T>A , CM000664.1:g.219746901T>A	GRCh37
NC_000002.10:g.219455145T>A	NCBI36
NG_012179.1:g.6647T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.132T>A MANE Select	ENSP00000258411.3:p.Ile44=
ENST00000258411.7:c.132T>A	ENSP00000258411.3:p.Ile44=
ENST00000458582.1:c.19T>A
NM_025216.2:c.132T>A	NP_079492.2:p.Ile44=
XM_011511928.1:c.81T>A	XP_011510230.1:p.Ile27=
XM_011511929.1:c.36T>A	XP_011510231.1:p.Ile12=
XM_011511930.1:c.132T>A	XP_011510232.1:p.Ile44=
XM_011511929.2:c.36T>A	XP_011510231.1:p.Ile12=
NM_025216.3:c.132T>A MANE Select	NP_079492.2:p.Ile44=