Canonical Allele Identifier: CA350618639

Gene: WNT10A

Linked Data

• dbSNP Id: rs1402476029
• MyVariant Identifiers: chr2:g.219747002A>C (hg19) ; chr2:g.218882280A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882280A>C , CM000664.2:g.218882280A>C	GRCh38
NC_000002.11:g.219747002A>C , CM000664.1:g.219747002A>C	GRCh37
NC_000002.10:g.219455246A>C	NCBI36
NG_012179.1:g.6748A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.233A>C MANE Select	ENSP00000258411.3:p.His78Pro
ENST00000258411.7:c.233A>C	ENSP00000258411.3:p.His78Pro
ENST00000458582.1:c.120A>C
NM_025216.2:c.233A>C	NP_079492.2:p.His78Pro
XM_011511928.1:c.182A>C	XP_011510230.1:p.His61Pro
XM_011511929.1:c.137A>C	XP_011510231.1:p.His46Pro
XM_011511930.1:c.233A>C	XP_011510232.1:p.His78Pro
XM_011511929.2:c.137A>C	XP_011510231.1:p.His46Pro
NM_025216.3:c.233A>C MANE Select	NP_079492.2:p.His78Pro