Canonical Allele Identifier: CA2618596093

Gene: WNT10B

Linked Data

• gnomAD v4: 12-48966074-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48966078del , CM000674.2:g.48966078del	GRCh38
NC_000012.11:g.49359861del , CM000674.1:g.49359861del	GRCh37
NC_000012.10:g.47646128del	NCBI36
NG_023347.1:g.10784del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301061.9:c.*20del MANE Select	ENSP00000301061.4:n.*20del
ENST00000301061.8:c.*20del	ENSP00000301061.4:n.*20del
ENST00000403957.5:c.*472del	ENSP00000385980.1:n.*472del
ENST00000407467.5:c.*472del	ENSP00000384691.1:n.*472del
NM_003394.3:c.*20del	NP_003385.2:n.*20del
XM_011538721.1:c.*20del	XP_011537023.1:n.*20del
XM_011538722.1:c.*20del	XP_011537024.1:n.*20del
XM_017019919.1:c.*20del	XP_016875408.1:n.*20del
XM_024449179.1:c.*20del	XP_024304947.1:n.*20del
NM_003394.4:c.*20del MANE Select	NP_003385.2:n.*20del