Canonical Allele Identifier: CA350618042

Gene: WNT10A

Linked Data

• dbSNP Id: rs2106011468
• MyVariant Identifiers: chr2:g.219746897A>T (hg19) ; chr2:g.218882175A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882175A>T , CM000664.2:g.218882175A>T	GRCh38
NC_000002.11:g.219746897A>T , CM000664.1:g.219746897A>T	GRCh37
NC_000002.10:g.219455141A>T	NCBI36
NG_012179.1:g.6643A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.128A>T MANE Select	ENSP00000258411.3:p.Asp43Val
ENST00000258411.7:c.128A>T	ENSP00000258411.3:p.Asp43Val
ENST00000458582.1:c.15A>T
NM_025216.2:c.128A>T	NP_079492.2:p.Asp43Val
XM_011511928.1:c.77A>T	XP_011510230.1:p.Asp26Val
XM_011511929.1:c.32A>T	XP_011510231.1:p.Asp11Val
XM_011511930.1:c.128A>T	XP_011510232.1:p.Asp43Val
XM_011511929.2:c.32A>T	XP_011510231.1:p.Asp11Val
NM_025216.3:c.128A>T MANE Select	NP_079492.2:p.Asp43Val