Canonical Allele Identifier: CA2607443043

Gene: WNT10A

Linked Data

• dbSNP Id: rs2106019046
• gnomAD v3: 2-218893372-AAG-A
• gnomAD v4: 2-218893372-AAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893375_218893376del , CM000664.2:g.218893375_218893376del	GRCh38
NC_000002.11:g.219758097_219758098del , CM000664.1:g.219758097_219758098del	GRCh37
NC_000002.10:g.219466341_219466342del	NCBI36
NG_012179.1:g.17843_17844del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.*104_*105del MANE Select	ENSP00000258411.3:n.*104_*105del
ENST00000258411.7:c.*104_*105del	ENSP00000258411.3:n.*104_*105del
ENST00000489887.1:n.47+108_47+109del
NM_025216.2:c.*104_*105del	NP_079492.2:n.*104_*105del
XM_011511928.1:c.*104_*105del	XP_011510230.1:n.*104_*105del
XM_011511929.1:c.*104_*105del	XP_011510231.1:n.*104_*105del
XM_011511930.1:c.*78_*79del	XP_011510232.1:n.*78_*79del
XM_011511929.2:c.*104_*105del	XP_011510231.1:n.*104_*105del
NM_025216.3:c.*104_*105del MANE Select	NP_079492.2:n.*104_*105del