Canonical Allele Identifier: CA2515322910

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218881805G>C , CM000664.2:g.218881805G>C	GRCh38
NC_000002.11:g.219746527G>C , CM000664.1:g.219746527G>C	GRCh37
NC_000002.10:g.219454771G>C	NCBI36
NG_012179.1:g.6273G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.114-356G>C MANE Select	ENSP00000258411.3:n.114-356G>C
ENST00000258411.7:c.114-356G>C	ENSP00000258411.3:n.114-356G>C
NM_025216.2:c.114-356G>C	NP_079492.2:n.114-356G>C
XM_011511928.1:c.62+338G>C	XP_011510230.1:n.62+338G>C
XM_011511929.1:c.18-356G>C	XP_011510231.1:n.18-356G>C
XM_011511930.1:c.114-356G>C	XP_011510232.1:n.114-356G>C
XM_011511929.2:c.18-356G>C	XP_011510231.1:n.18-356G>C
NM_025216.3:c.114-356G>C MANE Select	NP_079492.2:n.114-356G>C