Canonical Allele Identifier: CA1328961558

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882262T= , CM000664.2:g.218882262T=	GRCh38
NC_000002.11:g.219746984T= , CM000664.1:g.219746984T=	GRCh37
NC_000002.10:g.219455228T=	NCBI36
NG_012179.1:g.6730T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.215T= MANE Select	ENSP00000258411.3:p.Met72=
ENST00000258411.7:c.215T=	ENSP00000258411.3:p.Met72=
ENST00000458582.1:c.102T=
NM_025216.2:c.215T=	NP_079492.2:p.Met72=
XM_011511928.1:c.164T=	XP_011510230.1:p.Met55=
XM_011511929.1:c.119T=	XP_011510231.1:p.Met40=
XM_011511930.1:c.215T=	XP_011510232.1:p.Met72=
XM_011511929.2:c.119T=	XP_011510231.1:p.Met40=
NM_025216.3:c.215T= MANE Select	NP_079492.2:p.Met72=