Canonical Allele Identifier: CA2754310714

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882124_218882125dup , CM000664.2:g.218882124_218882125dup	GRCh38
NC_000002.11:g.219746846_219746847dup , CM000664.1:g.219746846_219746847dup	GRCh37
NC_000002.10:g.219455090_219455091dup	NCBI36
NG_012179.1:g.6592_6593dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.114-37_114-36dup MANE Select	ENSP00000258411.3:n.114-37_114-36dup
ENST00000258411.7:c.114-37_114-36dup	ENSP00000258411.3:n.114-37_114-36dup
NM_025216.2:c.114-37_114-36dup	NP_079492.2:n.114-37_114-36dup
XM_011511928.1:c.63-37_63-36dup	XP_011510230.1:n.63-37_63-36dup
XM_011511929.1:c.18-37_18-36dup	XP_011510231.1:n.18-37_18-36dup
XM_011511930.1:c.114-37_114-36dup	XP_011510232.1:n.114-37_114-36dup
XM_011511929.2:c.18-37_18-36dup	XP_011510231.1:n.18-37_18-36dup
NM_025216.3:c.114-37_114-36dup MANE Select	NP_079492.2:n.114-37_114-36dup