Canonical Allele Identifier: CA2663174677

Gene: WNT10A

Linked Data

• gnomAD v4: 2-218893375-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893375A>G , CM000664.2:g.218893375A>G	GRCh38
NC_000002.11:g.219758097A>G , CM000664.1:g.219758097A>G	GRCh37
NC_000002.10:g.219466341A>G	NCBI36
NG_012179.1:g.17843A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.*104A>G MANE Select	ENSP00000258411.3:n.*104A>G
ENST00000258411.7:c.*104A>G	ENSP00000258411.3:n.*104A>G
ENST00000489887.1:n.47+108A>G
NM_025216.2:c.*104A>G	NP_079492.2:n.*104A>G
XM_011511928.1:c.*104A>G	XP_011510230.1:n.*104A>G
XM_011511929.1:c.*104A>G	XP_011510231.1:n.*104A>G
XM_011511930.1:c.*78A>G	XP_011510232.1:n.*78A>G
XM_011511929.2:c.*104A>G	XP_011510231.1:n.*104A>G
NM_025216.3:c.*104A>G MANE Select	NP_079492.2:n.*104A>G