Canonical Allele Identifier: CA2618596021

Gene: WNT10B

Linked Data

• gnomAD v4: 12-48965981-ATACTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48965984_48965988del , CM000674.2:g.48965984_48965988del	GRCh38
NC_000012.11:g.49359767_49359771del , CM000674.1:g.49359767_49359771del	GRCh37
NC_000012.10:g.47646034_47646038del	NCBI36
NG_023347.1:g.10873_10877del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301061.9:c.*109_*113del MANE Select	ENSP00000301061.4:n.*109_*113del
ENST00000301061.8:c.*109_*113del	ENSP00000301061.4:n.*109_*113del
ENST00000403957.5:c.*561_*565del	ENSP00000385980.1:n.*561_*565del
ENST00000407467.5:c.*561_*565del	ENSP00000384691.1:n.*561_*565del
NM_003394.3:c.*109_*113del	NP_003385.2:n.*109_*113del
XM_011538721.1:c.*109_*113del	XP_011537023.1:n.*109_*113del
XM_011538722.1:c.*109_*113del	XP_011537024.1:n.*109_*113del
XM_017019919.1:c.*109_*113del	XP_016875408.1:n.*109_*113del
XM_024449179.1:c.*109_*113del	XP_024304947.1:n.*109_*113del
NM_003394.4:c.*109_*113del MANE Select	NP_003385.2:n.*109_*113del