Canonical Allele Identifier: CA1739107510

Gene: WNT16

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.121334754_121334755delinsAT , CM000669.2:g.121334754_121334755delinsAT	GRCh38
NC_000007.13:g.120974808_120974809delinsAT , CM000669.1:g.120974808_120974809delinsAT	GRCh37
NC_000007.12:g.120762044_120762045delinsAT	NCBI36
NG_029242.1:g.14388_14389delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222462.3:c.633+2790_633+2791delinsAT MANE Select	ENSP00000222462.2:n.633+2790_633+2791delinsAT
ENST00000222462.2:c.633+2790_633+2791delinsAT	ENSP00000222462.2:n.633+2790_633+2791delinsAT
ENST00000361301.6:c.603+2790_603+2791delinsAT	ENSP00000355065.2:n.603+2790_603+2791delinsAT
NM_016087.2:c.603+2790_603+2791delinsAT	NP_057171.2:n.603+2790_603+2791delinsAT
NM_057168.1:c.633+2790_633+2791delinsAT	NP_476509.1:n.633+2790_633+2791delinsAT
NM_057168.2:c.633+2790_633+2791delinsAT MANE Select	NP_476509.1:n.633+2790_633+2791delinsAT