Canonical Allele Identifier: CA65849780

Gene: WNT10A

Linked Data

• dbSNP Id: rs1041362666
• gnomAD v2: 2-219746432-GTC-G
• gnomAD v3: 2-218881710-GTC-G
• gnomAD v4: 2-218881710-GTC-G
• MyVariant Identifiers: chr2:g.219746433_219746434del (hg19) ; chr2:g.218881711_218881712del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218881712_218881713del , CM000664.2:g.218881712_218881713del	GRCh38
NC_000002.11:g.219746434_219746435del , CM000664.1:g.219746434_219746435del	GRCh37
NC_000002.10:g.219454678_219454679del	NCBI36
NG_012179.1:g.6180_6181del

Transcript Alleles

HGVS	Amino-acid change
ENST00000258411.8:c.114-449_114-448del MANE Select	ENSP00000258411.3:n.114-449_114-448del
ENST00000258411.7:c.114-449_114-448del	ENSP00000258411.3:n.114-449_114-448del
NM_025216.2:c.114-449_114-448del	NP_079492.2:n.114-449_114-448del
XM_011511928.1:c.62+245_62+246del	XP_011510230.1:n.62+245_62+246del
XM_011511929.1:c.18-449_18-448del	XP_011510231.1:n.18-449_18-448del
XM_011511930.1:c.114-449_114-448del	XP_011510232.1:n.114-449_114-448del
XM_011511929.2:c.18-449_18-448del	XP_011510231.1:n.18-449_18-448del
NM_025216.3:c.114-449_114-448del MANE Select	NP_079492.2:n.114-449_114-448del