Canonical Allele Identifier: CA764938285

Gene: WNT10A

Linked Data

• dbSNP Id: rs914277653
• gnomAD v3: 2-218881700-TTG-T
• gnomAD v4: 2-218881700-TTG-T
• MyVariant Identifiers: chr2:g.219746423_219746424del (hg19) ; chr2:g.218881701_218881702del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218881710_218881711del , CM000664.2:g.218881710_218881711del	GRCh38
NC_000002.11:g.219746432_219746433del , CM000664.1:g.219746432_219746433del	GRCh37
NC_000002.10:g.219454676_219454677del	NCBI36
NG_012179.1:g.6178_6179del

Transcript Alleles

HGVS	Amino-acid change
ENST00000258411.8:c.114-451_114-450del MANE Select	ENSP00000258411.3:n.114-451_114-450del
ENST00000258411.7:c.114-451_114-450del	ENSP00000258411.3:n.114-451_114-450del
NM_025216.2:c.114-451_114-450del	NP_079492.2:n.114-451_114-450del
XM_011511928.1:c.62+243_62+244del	XP_011510230.1:n.62+243_62+244del
XM_011511929.1:c.18-451_18-450del	XP_011510231.1:n.18-451_18-450del
XM_011511930.1:c.114-451_114-450del	XP_011510232.1:n.114-451_114-450del
XM_011511929.2:c.18-451_18-450del	XP_011510231.1:n.18-451_18-450del
NM_025216.3:c.114-451_114-450del MANE Select	NP_079492.2:n.114-451_114-450del