Canonical Allele Identifier: CA1328961289

Gene: WNT10A

Linked Data

• dbSNP Id: rs1944517857

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218881679C>T , CM000664.2:g.218881679C>T	GRCh38
NC_000002.11:g.219746401C>T , CM000664.1:g.219746401C>T	GRCh37
NC_000002.10:g.219454645C>T	NCBI36
NG_012179.1:g.6147C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.114-482C>T MANE Select	ENSP00000258411.3:n.114-482C>T
ENST00000258411.7:c.114-482C>T	ENSP00000258411.3:n.114-482C>T
NM_025216.2:c.114-482C>T	NP_079492.2:n.114-482C>T
XM_011511928.1:c.62+212C>T	XP_011510230.1:n.62+212C>T
XM_011511929.1:c.18-482C>T	XP_011510231.1:n.18-482C>T
XM_011511930.1:c.114-482C>T	XP_011510232.1:n.114-482C>T
XM_011511929.2:c.18-482C>T	XP_011510231.1:n.18-482C>T
NM_025216.3:c.114-482C>T MANE Select	NP_079492.2:n.114-482C>T