Canonical Allele Identifier: CA2113854

Gene: WNT10A

Linked Data

• ClinVar Variation Id: 1155709
• ClinVar RCV Id: RCV001498137
• dbSNP Id: rs753324320
• ExAC: 2:219746968 C / T
• gnomAD v2: 2-219746968-C-T
• gnomAD v4: 2-218882246-C-T
• MyVariant Identifiers: chr2:g.219746968C>T (hg19) ; chr2:g.218882246C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882246C>T , CM000664.2:g.218882246C>T	GRCh38
NC_000002.11:g.219746968C>T , CM000664.1:g.219746968C>T	GRCh37
NC_000002.10:g.219455212C>T	NCBI36
NG_012179.1:g.6714C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.199C>T MANE Select	ENSP00000258411.3:p.Leu67=
ENST00000258411.7:c.199C>T	ENSP00000258411.3:p.Leu67=
ENST00000458582.1:c.86C>T
NM_025216.2:c.199C>T	NP_079492.2:p.Leu67=
XM_011511928.1:c.148C>T	XP_011510230.1:p.Leu50=
XM_011511929.1:c.103C>T	XP_011510231.1:p.Leu35=
XM_011511930.1:c.199C>T	XP_011510232.1:p.Leu67=
XM_011511929.2:c.103C>T	XP_011510231.1:p.Leu35=
NM_025216.3:c.199C>T MANE Select	NP_079492.2:p.Leu67=