Canonical Allele Identifier: CA764944226

Gene: WNT10A

Linked Data

• dbSNP Id: rs1302612850
• MyVariant Identifiers: chr2:g.219758130C>T (hg19) ; chr2:g.218893408C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893408C>T , CM000664.2:g.218893408C>T	GRCh38
NC_000002.11:g.219758130C>T , CM000664.1:g.219758130C>T	GRCh37
NC_000002.10:g.219466374C>T	NCBI36
NG_012179.1:g.17876C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.*137C>T MANE Select	ENSP00000258411.3:n.*137C>T
ENST00000258411.7:c.*137C>T	ENSP00000258411.3:n.*137C>T
ENST00000489887.1:n.47+141C>T
NM_025216.2:c.*137C>T	NP_079492.2:n.*137C>T
XM_011511928.1:c.*137C>T	XP_011510230.1:n.*137C>T
XM_011511929.1:c.*137C>T	XP_011510231.1:n.*137C>T
XM_011511930.1:c.*111C>T	XP_011510232.1:n.*111C>T
XM_011511929.2:c.*137C>T	XP_011510231.1:n.*137C>T
NM_025216.3:c.*137C>T MANE Select	NP_079492.2:n.*137C>T