Canonical Allele Identifier: CA1042495632

Gene: WNT10A

Linked Data

• dbSNP Id: rs1944517568
• gnomAD v3: 2-218881659-AATGT-A
• gnomAD v4: 2-218881659-AATGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218881664_218881667del , CM000664.2:g.218881664_218881667del	GRCh38
NC_000002.11:g.219746386_219746389del , CM000664.1:g.219746386_219746389del	GRCh37
NC_000002.10:g.219454630_219454633del	NCBI36
NG_012179.1:g.6132_6135del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.114-497_114-494del MANE Select	ENSP00000258411.3:n.114-497_114-494del
ENST00000258411.7:c.114-497_114-494del	ENSP00000258411.3:n.114-497_114-494del
NM_025216.2:c.114-497_114-494del	NP_079492.2:n.114-497_114-494del
XM_011511928.1:c.62+197_62+200del	XP_011510230.1:n.62+197_62+200del
XM_011511929.1:c.18-497_18-494del	XP_011510231.1:n.18-497_18-494del
XM_011511930.1:c.114-497_114-494del	XP_011510232.1:n.114-497_114-494del
XM_011511929.2:c.18-497_18-494del	XP_011510231.1:n.18-497_18-494del
NM_025216.3:c.114-497_114-494del MANE Select	NP_079492.2:n.114-497_114-494del