Canonical Allele Identifier: CA350592122

Gene: WNT10A

Linked Data

• MyVariant Identifiers: chr2:g.219757901C>G (hg19) ; chr2:g.218893179C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893179C>G , CM000664.2:g.218893179C>G	GRCh38
NC_000002.11:g.219757901C>G , CM000664.1:g.219757901C>G	GRCh37
NC_000002.10:g.219466145C>G	NCBI36
NG_012179.1:g.17647C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1162C>G MANE Select	ENSP00000258411.3:p.Arg388Gly
ENST00000258411.7:c.1162C>G	ENSP00000258411.3:p.Arg388Gly
NM_025216.2:c.1162C>G	NP_079492.2:p.Arg388Gly
XM_011511928.1:c.1111C>G	XP_011510230.1:p.Arg371Gly
XM_011511929.1:c.1066C>G	XP_011510231.1:p.Arg356Gly
XM_011511930.1:c.782C>G	XP_011510232.1:p.Ala261Gly
XM_011511929.2:c.1066C>G	XP_011510231.1:p.Arg356Gly
NM_025216.3:c.1162C>G MANE Select	NP_079492.2:p.Arg388Gly