Canonical Allele Identifier: CA2843142785

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893254del , CM000664.2:g.218893254del	GRCh38
NC_000002.11:g.219757976del , CM000664.1:g.219757976del	GRCh37
NC_000002.10:g.219466220del	NCBI36
NG_012179.1:g.17722del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1237del MANE Select	ENSP00000258411.3:p.Val413SerfsTer25
ENST00000258411.7:c.1237del	ENSP00000258411.3:p.Val413SerfsTer25
ENST00000489887.1:n.34del
NM_025216.2:c.1237del	NP_079492.2:p.Val413SerfsTer25
XM_011511928.1:c.1186del	XP_011510230.1:p.Val396SerfsTer25
XM_011511929.1:c.1141del	XP_011510231.1:p.Val381SerfsTer25
XM_011511930.1:c.857del	XP_011510232.1:p.Gly286ValfsTer6
XM_011511929.2:c.1141del	XP_011510231.1:p.Val381SerfsTer25
NM_025216.3:c.1237del MANE Select	NP_079492.2:p.Val413SerfsTer25