Canonical Allele Identifier: CA2663173467

Gene: WNT10A

Linked Data

• gnomAD v4: 2-218882280-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882283del , CM000664.2:g.218882283del	GRCh38
NC_000002.11:g.219747005del , CM000664.1:g.219747005del	GRCh37
NC_000002.10:g.219455249del	NCBI36
NG_012179.1:g.6751del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.236del MANE Select	ENSP00000258411.3:p.Pro79LeufsTer?
ENST00000258411.7:c.236del	ENSP00000258411.3:p.Pro79LeufsTer?
ENST00000458582.1:c.123del
NM_025216.2:c.236del	NP_079492.2:p.Pro79LeufsTer?
XM_011511928.1:c.185del	XP_011510230.1:p.Pro62LeufsTer?
XM_011511929.1:c.140del	XP_011510231.1:p.Pro47LeufsTer?
XM_011511930.1:c.236del	XP_011510232.1:p.Pro79LeufsTer?
XM_011511929.2:c.140del	XP_011510231.1:p.Pro47LeufsTer?
NM_025216.3:c.236del MANE Select	NP_079492.2:p.Pro79LeufsTer?