Canonical Allele Identifier: CA350617969

Gene: WNT10A

Linked Data

• MyVariant Identifiers: chr2:g.219746887G>T (hg19) ; chr2:g.218882165G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882165G>T , CM000664.2:g.218882165G>T	GRCh38
NC_000002.11:g.219746887G>T , CM000664.1:g.219746887G>T	GRCh37
NC_000002.10:g.219455131G>T	NCBI36
NG_012179.1:g.6633G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.118G>T MANE Select	ENSP00000258411.3:p.Ala40Ser
ENST00000258411.7:c.118G>T	ENSP00000258411.3:p.Ala40Ser
ENST00000458582.1:c.5G>T
NM_025216.2:c.118G>T	NP_079492.2:p.Ala40Ser
XM_011511928.1:c.67G>T	XP_011510230.1:p.Ala23Ser
XM_011511929.1:c.22G>T	XP_011510231.1:p.Ala8Ser
XM_011511930.1:c.118G>T	XP_011510232.1:p.Ala40Ser
XM_011511929.2:c.22G>T	XP_011510231.1:p.Ala8Ser
NM_025216.3:c.118G>T MANE Select	NP_079492.2:p.Ala40Ser