Canonical Allele Identifier: CA1328965829

Gene: WNT10A

Linked Data

• dbSNP Id: rs1419603125
• gnomAD v4: 2-218893412-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893412G>T , CM000664.2:g.218893412G>T	GRCh38
NC_000002.11:g.219758134G>T , CM000664.1:g.219758134G>T	GRCh37
NC_000002.10:g.219466378G>T	NCBI36
NG_012179.1:g.17880G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.*141G>T MANE Select	ENSP00000258411.3:n.*141G>T
ENST00000258411.7:c.*141G>T	ENSP00000258411.3:n.*141G>T
ENST00000489887.1:n.47+145G>T
NM_025216.2:c.*141G>T	NP_079492.2:n.*141G>T
XM_011511928.1:c.*141G>T	XP_011510230.1:n.*141G>T
XM_011511929.1:c.*141G>T	XP_011510231.1:n.*141G>T
XM_011511930.1:c.*115G>T	XP_011510232.1:n.*115G>T
XM_011511929.2:c.*141G>T	XP_011510231.1:n.*141G>T
NM_025216.3:c.*141G>T MANE Select	NP_079492.2:n.*141G>T