Canonical Allele Identifier: CA2034911576

Gene: WNT10B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48965817_48965818delinsAG , CM000674.2:g.48965817_48965818delinsAG	GRCh38
NC_000012.11:g.49359600_49359601delinsAG , CM000674.1:g.49359600_49359601delinsAG	GRCh37
NC_000012.10:g.47645867_47645868delinsAG	NCBI36
NG_023347.1:g.11041_11042delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301061.9:c.*277_*278delinsCT MANE Select	ENSP00000301061.4:n.*277_*278delinsCT
ENST00000301061.8:c.*277_*278delinsCT	ENSP00000301061.4:n.*277_*278delinsCT
ENST00000403957.5:c.*729_*730delinsCT	ENSP00000385980.1:n.*729_*730delinsCT
ENST00000407467.5:c.*729_*730delinsCT	ENSP00000384691.1:n.*729_*730delinsCT
NM_003394.3:c.*277_*278delinsCT	NP_003385.2:n.*277_*278delinsCT
XM_011538721.1:c.*277_*278delinsCT	XP_011537023.1:n.*277_*278delinsCT
XM_011538722.1:c.*277_*278delinsCT	XP_011537024.1:n.*277_*278delinsCT
XM_017019919.1:c.*277_*278delinsCT	XP_016875408.1:n.*277_*278delinsCT
XM_024449179.1:c.*277_*278delinsCT	XP_024304947.1:n.*277_*278delinsCT
NM_003394.4:c.*277_*278delinsCT MANE Select	NP_003385.2:n.*277_*278delinsCT