Canonical Allele Identifier: CA2663174698

Gene: WNT10A

Linked Data

• gnomAD v4: 2-218893404-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893408dup , CM000664.2:g.218893408dup	GRCh38
NC_000002.11:g.219758130dup , CM000664.1:g.219758130dup	GRCh37
NC_000002.10:g.219466374dup	NCBI36
NG_012179.1:g.17876dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.*137dup MANE Select	ENSP00000258411.3:n.*137dup
ENST00000258411.7:c.*137dup	ENSP00000258411.3:n.*137dup
ENST00000489887.1:n.47+141dup
NM_025216.2:c.*137dup	NP_079492.2:n.*137dup
XM_011511928.1:c.*137dup	XP_011510230.1:n.*137dup
XM_011511929.1:c.*137dup	XP_011510231.1:n.*137dup
XM_011511930.1:c.*111dup	XP_011510232.1:n.*111dup
XM_011511929.2:c.*137dup	XP_011510231.1:n.*137dup
NM_025216.3:c.*137dup MANE Select	NP_079492.2:n.*137dup