Canonical Allele Identifier: CA65849996

Gene: WNT10A

Linked Data

• dbSNP Id: rs114813261
• MyVariant Identifiers: chr2:g.218881929G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218881929G>T , CM000664.2:g.218881929G>T	GRCh38
NC_000002.11:g.219746651G>T , CM000664.1:g.219746651G>T	GRCh37
NC_000002.10:g.219454895G>T	NCBI36
NG_012179.1:g.6397G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000258411.8:c.114-232G>T MANE Select	ENSP00000258411.3:n.114-232G>T
ENST00000258411.7:c.114-232G>T	ENSP00000258411.3:n.114-232G>T
NM_025216.2:c.114-232G>T	NP_079492.2:n.114-232G>T
XM_011511928.1:c.63-232G>T	XP_011510230.1:n.63-232G>T
XM_011511929.1:c.18-232G>T	XP_011510231.1:n.18-232G>T
XM_011511930.1:c.114-232G>T	XP_011510232.1:n.114-232G>T
XM_011511929.2:c.18-232G>T	XP_011510231.1:n.18-232G>T
NM_025216.3:c.114-232G>T MANE Select	NP_079492.2:n.114-232G>T