Canonical Allele Identifier: CA764944225

Gene: WNT10A

Linked Data

• dbSNP Id: rs1483544743
• gnomAD v3: 2-218893390-A-T
• gnomAD v4: 2-218893390-A-T
• MyVariant Identifiers: chr2:g.219758112A>T (hg19) ; chr2:g.218893390A>T (hg38)

Genomic Alleles

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

Transcript Alleles

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