Canonical Allele Identifier: CA431416801

Gene: WNT10A

Linked Data

• MyVariant Identifiers: chr2:g.219754986C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218890264C>T , CM000664.2:g.218890264C>T	GRCh38
NC_000002.11:g.219754986C>T , CM000664.1:g.219754986C>T	GRCh37
NC_000002.10:g.219463230C>T	NCBI36
NG_012179.1:g.14732C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000258411.8:c.657C>T MANE Select	ENSP00000258411.3:p.Gly219=
ENST00000258411.7:c.657C>T	ENSP00000258411.3:p.Gly219=
ENST00000458582.1:c.264-2510C>T
NM_025216.2:c.657C>T	NP_079492.2:p.Gly219=
XM_011511928.1:c.606C>T	XP_011510230.1:p.Gly202=
XM_011511929.1:c.561C>T	XP_011510231.1:p.Gly187=
XM_011511930.1:c.377-2510C>T	XP_011510232.1:n.377-2510C>T
XM_011511929.2:c.561C>T	XP_011510231.1:p.Gly187=
NM_025216.3:c.657C>T MANE Select	NP_079492.2:p.Gly219=