Canonical Allele Identifier: CA1328961404

Gene: WNT10A

Linked Data

• dbSNP Id: rs1944521573

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218881957_218881960del , CM000664.2:g.218881957_218881960del	GRCh38
NC_000002.11:g.219746679_219746682del , CM000664.1:g.219746679_219746682del	GRCh37
NC_000002.10:g.219454923_219454926del	NCBI36
NG_012179.1:g.6425_6428del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.114-204_114-201del MANE Select	ENSP00000258411.3:n.114-204_114-201del
ENST00000258411.7:c.114-204_114-201del	ENSP00000258411.3:n.114-204_114-201del
NM_025216.2:c.114-204_114-201del	NP_079492.2:n.114-204_114-201del
XM_011511928.1:c.63-204_63-201del	XP_011510230.1:n.63-204_63-201del
XM_011511929.1:c.18-204_18-201del	XP_011510231.1:n.18-204_18-201del
XM_011511930.1:c.114-204_114-201del	XP_011510232.1:n.114-204_114-201del
XM_011511929.2:c.18-204_18-201del	XP_011510231.1:n.18-204_18-201del
NM_025216.3:c.114-204_114-201del MANE Select	NP_079492.2:n.114-204_114-201del