Canonical Allele Identifier: CA1328965139

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218890260T= , CM000664.2:g.218890260T=	GRCh38
NC_000002.11:g.219754982T= , CM000664.1:g.219754982T=	GRCh37
NC_000002.10:g.219463226T=	NCBI36
NG_012179.1:g.14728T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000258411.8:c.653T= MANE Select	ENSP00000258411.3:p.Met218=
ENST00000258411.7:c.653T=	ENSP00000258411.3:p.Met218=
ENST00000458582.1:c.264-2514T=
NM_025216.2:c.653T=	NP_079492.2:p.Met218=
XM_011511928.1:c.602T=	XP_011510230.1:p.Met201=
XM_011511929.1:c.557T=	XP_011510231.1:p.Met186=
XM_011511930.1:c.377-2514T=	XP_011510232.1:n.377-2514T=
XM_011511929.2:c.557T=	XP_011510231.1:p.Met186=
NM_025216.3:c.653T= MANE Select	NP_079492.2:p.Met218=