Canonical Allele Identifier: CA2663174714

Gene: WNT10A

Linked Data

• gnomAD v4: 2-218893417-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893417G>T , CM000664.2:g.218893417G>T	GRCh38
NC_000002.11:g.219758139G>T , CM000664.1:g.219758139G>T	GRCh37
NC_000002.10:g.219466383G>T	NCBI36
NG_012179.1:g.17885G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.*146G>T MANE Select	ENSP00000258411.3:n.*146G>T
ENST00000258411.7:c.*146G>T	ENSP00000258411.3:n.*146G>T
ENST00000489887.1:n.47+150G>T
NM_025216.2:c.*146G>T	NP_079492.2:n.*146G>T
XM_011511928.1:c.*146G>T	XP_011510230.1:n.*146G>T
XM_011511929.1:c.*146G>T	XP_011510231.1:n.*146G>T
XM_011511930.1:c.*120G>T	XP_011510232.1:n.*120G>T
XM_011511929.2:c.*146G>T	XP_011510231.1:n.*146G>T
NM_025216.3:c.*146G>T MANE Select	NP_079492.2:n.*146G>T