Canonical Allele Identifier: CA1328961334

Gene: WNT10A

Linked Data

• dbSNP Id: rs1944519766

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218881765T>G , CM000664.2:g.218881765T>G	GRCh38
NC_000002.11:g.219746487T>G , CM000664.1:g.219746487T>G	GRCh37
NC_000002.10:g.219454731T>G	NCBI36
NG_012179.1:g.6233T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.114-396T>G MANE Select	ENSP00000258411.3:n.114-396T>G
ENST00000258411.7:c.114-396T>G	ENSP00000258411.3:n.114-396T>G
NM_025216.2:c.114-396T>G	NP_079492.2:n.114-396T>G
XM_011511928.1:c.62+298T>G	XP_011510230.1:n.62+298T>G
XM_011511929.1:c.18-396T>G	XP_011510231.1:n.18-396T>G
XM_011511930.1:c.114-396T>G	XP_011510232.1:n.114-396T>G
XM_011511929.2:c.18-396T>G	XP_011510231.1:n.18-396T>G
NM_025216.3:c.114-396T>G MANE Select	NP_079492.2:n.114-396T>G