Canonical Allele Identifier: CA2754311154

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893390A>G , CM000664.2:g.218893390A>G	GRCh38
NC_000002.11:g.219758112A>G , CM000664.1:g.219758112A>G	GRCh37
NC_000002.10:g.219466356A>G	NCBI36
NG_012179.1:g.17858A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.*119A>G MANE Select	ENSP00000258411.3:n.*119A>G
ENST00000258411.7:c.*119A>G	ENSP00000258411.3:n.*119A>G
ENST00000489887.1:n.47+123A>G
NM_025216.2:c.*119A>G	NP_079492.2:n.*119A>G
XM_011511928.1:c.*119A>G	XP_011510230.1:n.*119A>G
XM_011511929.1:c.*119A>G	XP_011510231.1:n.*119A>G
XM_011511930.1:c.*93A>G	XP_011510232.1:n.*93A>G
XM_011511929.2:c.*119A>G	XP_011510231.1:n.*119A>G
NM_025216.3:c.*119A>G MANE Select	NP_079492.2:n.*119A>G