Canonical Allele Identifier: CA350618007

Gene: WNT10A

Linked Data

• MyVariant Identifiers: chr2:g.219746891C>G (hg19) ; chr2:g.218882169C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882169C>G , CM000664.2:g.218882169C>G	GRCh38
NC_000002.11:g.219746891C>G , CM000664.1:g.219746891C>G	GRCh37
NC_000002.10:g.219455135C>G	NCBI36
NG_012179.1:g.6637C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.122C>G MANE Select	ENSP00000258411.3:p.Pro41Arg
ENST00000258411.7:c.122C>G	ENSP00000258411.3:p.Pro41Arg
ENST00000458582.1:c.9C>G
NM_025216.2:c.122C>G	NP_079492.2:p.Pro41Arg
XM_011511928.1:c.71C>G	XP_011510230.1:p.Pro24Arg
XM_011511929.1:c.26C>G	XP_011510231.1:p.Pro9Arg
XM_011511930.1:c.122C>G	XP_011510232.1:p.Pro41Arg
XM_011511929.2:c.26C>G	XP_011510231.1:p.Pro9Arg
NM_025216.3:c.122C>G MANE Select	NP_079492.2:p.Pro41Arg