Canonical Allele Identifier: CA350592089

Gene: WNT10A

Linked Data

• MyVariant Identifiers: chr2:g.219757898A>T (hg19) ; chr2:g.218893176A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893176A>T , CM000664.2:g.218893176A>T	GRCh38
NC_000002.11:g.219757898A>T , CM000664.1:g.219757898A>T	GRCh37
NC_000002.10:g.219466142A>T	NCBI36
NG_012179.1:g.17644A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1159A>T MANE Select	ENSP00000258411.3:p.Thr387Ser
ENST00000258411.7:c.1159A>T	ENSP00000258411.3:p.Thr387Ser
NM_025216.2:c.1159A>T	NP_079492.2:p.Thr387Ser
XM_011511928.1:c.1108A>T	XP_011510230.1:p.Thr370Ser
XM_011511929.1:c.1063A>T	XP_011510231.1:p.Thr355Ser
XM_011511930.1:c.779A>T	XP_011510232.1:p.Asp260Val
XM_011511929.2:c.1063A>T	XP_011510231.1:p.Thr355Ser
NM_025216.3:c.1159A>T MANE Select	NP_079492.2:p.Thr387Ser