Canonical Allele Identifier: CA350618522

Gene: WNT10A

Linked Data

• MyVariant Identifiers: chr2:g.219746982G>T (hg19) ; chr2:g.218882260G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882260G>T , CM000664.2:g.218882260G>T	GRCh38
NC_000002.11:g.219746982G>T , CM000664.1:g.219746982G>T	GRCh37
NC_000002.10:g.219455226G>T	NCBI36
NG_012179.1:g.6728G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.213G>T MANE Select	ENSP00000258411.3:p.Gln71His
ENST00000258411.7:c.213G>T	ENSP00000258411.3:p.Gln71His
ENST00000458582.1:c.100G>T
NM_025216.2:c.213G>T	NP_079492.2:p.Gln71His
XM_011511928.1:c.162G>T	XP_011510230.1:p.Gln54His
XM_011511929.1:c.117G>T	XP_011510231.1:p.Gln39His
XM_011511930.1:c.213G>T	XP_011510232.1:p.Gln71His
XM_011511929.2:c.117G>T	XP_011510231.1:p.Gln39His
NM_025216.3:c.213G>T MANE Select	NP_079492.2:p.Gln71His