Canonical Allele Identifier: CA431416454

Gene: WNT10A

Linked Data

• MyVariant Identifiers: chr2:g.219746967C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882245C>T , CM000664.2:g.218882245C>T	GRCh38
NC_000002.11:g.219746967C>T , CM000664.1:g.219746967C>T	GRCh37
NC_000002.10:g.219455211C>T	NCBI36
NG_012179.1:g.6713C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.198C>T MANE Select	ENSP00000258411.3:p.Gly66=
ENST00000258411.7:c.198C>T	ENSP00000258411.3:p.Gly66=
ENST00000458582.1:c.85C>T
NM_025216.2:c.198C>T	NP_079492.2:p.Gly66=
XM_011511928.1:c.147C>T	XP_011510230.1:p.Gly49=
XM_011511929.1:c.102C>T	XP_011510231.1:p.Gly34=
XM_011511930.1:c.198C>T	XP_011510232.1:p.Gly66=
XM_011511929.2:c.102C>T	XP_011510231.1:p.Gly34=
NM_025216.3:c.198C>T MANE Select	NP_079492.2:p.Gly66=