Canonical Allele Identifier: CA1328965833

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893424_218893428delinsGTGAT , CM000664.2:g.218893424_218893428delinsGTGAT	GRCh38
NC_000002.11:g.219758146_219758150delinsGTGAT , CM000664.1:g.219758146_219758150delinsGTGAT	GRCh37
NC_000002.10:g.219466390_219466394delinsGTGAT	NCBI36
NG_012179.1:g.17892_17896delinsGTGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.*153_*157delinsGTGAT MANE Select	ENSP00000258411.3:n.*153_*157delinsGTGAT
ENST00000258411.7:c.*153_*157delinsGTGAT	ENSP00000258411.3:n.*153_*157delinsGTGAT
ENST00000489887.1:n.47+157_47+161delinsGTGAT
NM_025216.2:c.*153_*157delinsGTGAT	NP_079492.2:n.*153_*157delinsGTGAT
XM_011511928.1:c.*153_*157delinsGTGAT	XP_011510230.1:n.*153_*157delinsGTGAT
XM_011511929.1:c.*153_*157delinsGTGAT	XP_011510231.1:n.*153_*157delinsGTGAT
XM_011511930.1:c.*127_*131delinsGTGAT	XP_011510232.1:n.*127_*131delinsGTGAT
XM_011511929.2:c.*153_*157delinsGTGAT	XP_011510231.1:n.*153_*157delinsGTGAT
NM_025216.3:c.*153_*157delinsGTGAT MANE Select	NP_079492.2:n.*153_*157delinsGTGAT