Canonical Allele Identifier: CA2114130

Gene: WNT10A

Linked Data

• dbSNP Id: rs758910410
• ExAC: 2:219757996 G / T
• gnomAD v2: 2-219757996-G-T
• gnomAD v4: 2-218893274-G-T
• MyVariant Identifiers: chr2:g.219757996G>T (hg19) ; chr2:g.218893274G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893274G>T , CM000664.2:g.218893274G>T	GRCh38
NC_000002.11:g.219757996G>T , CM000664.1:g.219757996G>T	GRCh37
NC_000002.10:g.219466240G>T	NCBI36
NG_012179.1:g.17742G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000258411.8:c.*3G>T MANE Select	ENSP00000258411.3:n.*3G>T
ENST00000258411.7:c.*3G>T	ENSP00000258411.3:n.*3G>T
ENST00000489887.1:n.47+7G>T
NM_025216.2:c.*3G>T	NP_079492.2:n.*3G>T
XM_011511928.1:c.*3G>T	XP_011510230.1:n.*3G>T
XM_011511929.1:c.*3G>T	XP_011510231.1:n.*3G>T
XM_011511930.1:c.877G>T	XP_011510232.1:p.Gly293Cys
XM_011511929.2:c.*3G>T	XP_011510231.1:n.*3G>T
NM_025216.3:c.*3G>T MANE Select	NP_079492.2:n.*3G>T