Canonical Allele Identifier: CA539621549

Gene: WNT10A

Linked Data

• dbSNP Id: rs1194588339
• gnomAD v2: 2-219746428-GTGTGTC-G
• gnomAD v3: 2-218881706-GTGTGTC-G
• gnomAD v4: 2-218881706-GTGTGTC-G
• MyVariant Identifiers: chr2:g.219746429_219746434del (hg19) ; chr2:g.218881707_218881712del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218881710_218881715del , CM000664.2:g.218881710_218881715del	GRCh38
NC_000002.11:g.219746432_219746437del , CM000664.1:g.219746432_219746437del	GRCh37
NC_000002.10:g.219454676_219454681del	NCBI36
NG_012179.1:g.6178_6183del

Transcript Alleles

HGVS	Amino-acid change
ENST00000258411.8:c.114-451_114-446del MANE Select	ENSP00000258411.3:n.114-451_114-446del
ENST00000258411.7:c.114-451_114-446del	ENSP00000258411.3:n.114-451_114-446del
NM_025216.2:c.114-451_114-446del	NP_079492.2:n.114-451_114-446del
XM_011511928.1:c.62+243_62+248del	XP_011510230.1:n.62+243_62+248del
XM_011511929.1:c.18-451_18-446del	XP_011510231.1:n.18-451_18-446del
XM_011511930.1:c.114-451_114-446del	XP_011510232.1:n.114-451_114-446del
XM_011511929.2:c.18-451_18-446del	XP_011510231.1:n.18-451_18-446del
NM_025216.3:c.114-451_114-446del MANE Select	NP_079492.2:n.114-451_114-446del