Canonical Allele Identifier: CA350618350

Gene: WNT10A

Linked Data

• gnomAD v4: 2-218882228-T-C
• MyVariant Identifiers: chr2:g.219746950T>C (hg19) ; chr2:g.218882228T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882228T>C , CM000664.2:g.218882228T>C	GRCh38
NC_000002.11:g.219746950T>C , CM000664.1:g.219746950T>C	GRCh37
NC_000002.10:g.219455194T>C	NCBI36
NG_012179.1:g.6696T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.181T>C MANE Select	ENSP00000258411.3:p.Cys61Arg
ENST00000258411.7:c.181T>C	ENSP00000258411.3:p.Cys61Arg
ENST00000458582.1:c.68T>C
NM_025216.2:c.181T>C	NP_079492.2:p.Cys61Arg
XM_011511928.1:c.130T>C	XP_011510230.1:p.Cys44Arg
XM_011511929.1:c.85T>C	XP_011510231.1:p.Cys29Arg
XM_011511930.1:c.181T>C	XP_011510232.1:p.Cys61Arg
XM_011511929.2:c.85T>C	XP_011510231.1:p.Cys29Arg
NM_025216.3:c.181T>C MANE Select	NP_079492.2:p.Cys61Arg