Canonical Allele Identifier: CA2113852

Gene: WNT10A

Linked Data

• dbSNP Id: rs771002314
• ExAC: 2:219746940 CA / C
• gnomAD v2: 2-219746940-CA-C
• MyVariant Identifiers: chr2:g.219746941del (hg19) ; chr2:g.218882220del (hg38) ; chr2:g.218882219del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882220del , CM000664.2:g.218882220del	GRCh38
NC_000002.11:g.219746942del , CM000664.1:g.219746942del	GRCh37
NC_000002.10:g.219455186del	NCBI36
NG_012179.1:g.6688del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.173del MANE Select	ENSP00000258411.3:p.Asn58ThrfsTer5
ENST00000258411.7:c.173del	ENSP00000258411.3:p.Asn58ThrfsTer5
ENST00000458582.1:c.60del
NM_025216.2:c.173del	NP_079492.2:p.Asn58ThrfsTer5
XM_011511928.1:c.122del	XP_011510230.1:p.Asn41ThrfsTer5
XM_011511929.1:c.77del	XP_011510231.1:p.Asn26ThrfsTer5
XM_011511930.1:c.173del	XP_011510232.1:p.Asn58ThrfsTer5
XM_011511929.2:c.77del	XP_011510231.1:p.Asn26ThrfsTer5
NM_025216.3:c.173del MANE Select	NP_079492.2:p.Asn58ThrfsTer5