Canonical Allele Identifier: CA2663174682

Gene: WNT10A

Linked Data

• gnomAD v4: 2-218893379-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893379G>T , CM000664.2:g.218893379G>T	GRCh38
NC_000002.11:g.219758101G>T , CM000664.1:g.219758101G>T	GRCh37
NC_000002.10:g.219466345G>T	NCBI36
NG_012179.1:g.17847G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.*108G>T MANE Select	ENSP00000258411.3:n.*108G>T
ENST00000258411.7:c.*108G>T	ENSP00000258411.3:n.*108G>T
ENST00000489887.1:n.47+112G>T
NM_025216.2:c.*108G>T	NP_079492.2:n.*108G>T
XM_011511928.1:c.*108G>T	XP_011510230.1:n.*108G>T
XM_011511929.1:c.*108G>T	XP_011510231.1:n.*108G>T
XM_011511930.1:c.*82G>T	XP_011510232.1:n.*82G>T
XM_011511929.2:c.*108G>T	XP_011510231.1:n.*108G>T
NM_025216.3:c.*108G>T MANE Select	NP_079492.2:n.*108G>T