Canonical Allele Identifier: CA1328965665

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893258G= , CM000664.2:g.218893258G=	GRCh38
NC_000002.11:g.219757980G= , CM000664.1:g.219757980G=	GRCh37
NC_000002.10:g.219466224G=	NCBI36
NG_012179.1:g.17726G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1241G= MANE Select	ENSP00000258411.3:p.Ser414=
ENST00000258411.7:c.1241G=	ENSP00000258411.3:p.Ser414=
ENST00000489887.1:n.38G=
NM_025216.2:c.1241G=	NP_079492.2:p.Ser414=
XM_011511928.1:c.1190G=	XP_011510230.1:p.Ser397=
XM_011511929.1:c.1145G=	XP_011510231.1:p.Ser382=
XM_011511930.1:c.861G=	XP_011510232.1:p.Gln287=
XM_011511929.2:c.1145G=	XP_011510231.1:p.Ser382=
NM_025216.3:c.1241G= MANE Select	NP_079492.2:p.Ser414=