Canonical Allele Identifier: CA2577276401

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893199_218893210dup , CM000664.2:g.218893199_218893210dup	GRCh38
NC_000002.11:g.219757921_219757932dup , CM000664.1:g.219757921_219757932dup	GRCh37
NC_000002.10:g.219466165_219466176dup	NCBI36
NG_012179.1:g.17667_17678dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1182_1193dup MANE Select	ENSP00000258411.3:p.His397_Trp398insCysArgPheHis
ENST00000258411.7:c.1182_1193dup	ENSP00000258411.3:p.His397_Trp398insCysArgPheHis
NM_025216.2:c.1182_1193dup	NP_079492.2:p.His397_Trp398insCysArgPheHis
XM_011511928.1:c.1131_1142dup	XP_011510230.1:p.His380_Trp381insCysArgPheHis
XM_011511929.1:c.1086_1097dup	XP_011510231.1:p.His365_Trp366insCysArgPheHis
XM_011511930.1:c.802_813dup	XP_011510232.1:p.Leu271_Val272insProLeuProLeu
XM_011511929.2:c.1086_1097dup	XP_011510231.1:p.His365_Trp366insCysArgPheHis
NM_025216.3:c.1182_1193dup MANE Select	NP_079492.2:p.His397_Trp398insCysArgPheHis