Canonical Allele Identifier: CA2034911555

Gene: WNT10B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48965777_48965778delinsAG , CM000674.2:g.48965777_48965778delinsAG	GRCh38
NC_000012.11:g.49359560_49359561delinsAG , CM000674.1:g.49359560_49359561delinsAG	GRCh37
NC_000012.10:g.47645827_47645828delinsAG	NCBI36
NG_023347.1:g.11081_11082delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301061.9:c.*317_*318delinsCT MANE Select	ENSP00000301061.4:n.*317_*318delinsCT
ENST00000301061.8:c.*317_*318delinsCT	ENSP00000301061.4:n.*317_*318delinsCT
ENST00000403957.5:c.*769_*770delinsCT	ENSP00000385980.1:n.*769_*770delinsCT
ENST00000407467.5:c.*769_*770delinsCT	ENSP00000384691.1:n.*769_*770delinsCT
NM_003394.3:c.*317_*318delinsCT	NP_003385.2:n.*317_*318delinsCT
XM_011538721.1:c.*317_*318delinsCT	XP_011537023.1:n.*317_*318delinsCT
XM_011538722.1:c.*317_*318delinsCT	XP_011537024.1:n.*317_*318delinsCT
XM_017019919.1:c.*317_*318delinsCT	XP_016875408.1:n.*317_*318delinsCT
XM_024449179.1:c.*317_*318delinsCT	XP_024304947.1:n.*317_*318delinsCT
NM_003394.4:c.*317_*318delinsCT MANE Select	NP_003385.2:n.*317_*318delinsCT