Canonical Allele Identifier: CA350618388

Gene: WNT10A

Linked Data

• MyVariant Identifiers: chr2:g.219746957C>T (hg19) ; chr2:g.218882235C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882235C>T , CM000664.2:g.218882235C>T	GRCh38
NC_000002.11:g.219746957C>T , CM000664.1:g.219746957C>T	GRCh37
NC_000002.10:g.219455201C>T	NCBI36
NG_012179.1:g.6703C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.188C>T MANE Select	ENSP00000258411.3:p.Thr63Ile
ENST00000258411.7:c.188C>T	ENSP00000258411.3:p.Thr63Ile
ENST00000458582.1:c.75C>T
NM_025216.2:c.188C>T	NP_079492.2:p.Thr63Ile
XM_011511928.1:c.137C>T	XP_011510230.1:p.Thr46Ile
XM_011511929.1:c.92C>T	XP_011510231.1:p.Thr31Ile
XM_011511930.1:c.188C>T	XP_011510232.1:p.Thr63Ile
XM_011511929.2:c.92C>T	XP_011510231.1:p.Thr31Ile
NM_025216.3:c.188C>T MANE Select	NP_079492.2:p.Thr63Ile