Canonical Allele Identifier: CA2618595848

Gene: WNT10B

Linked Data

• gnomAD v4: 12-48965819-TGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48965821_48965822del , CM000674.2:g.48965821_48965822del	GRCh38
NC_000012.11:g.49359604_49359605del , CM000674.1:g.49359604_49359605del	GRCh37
NC_000012.10:g.47645871_47645872del	NCBI36
NG_023347.1:g.11038_11039del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301061.9:c.*274_*275del MANE Select	ENSP00000301061.4:n.*274_*275del
ENST00000301061.8:c.*274_*275del	ENSP00000301061.4:n.*274_*275del
ENST00000403957.5:c.*726_*727del	ENSP00000385980.1:n.*726_*727del
ENST00000407467.5:c.*726_*727del	ENSP00000384691.1:n.*726_*727del
NM_003394.3:c.*274_*275del	NP_003385.2:n.*274_*275del
XM_011538721.1:c.*274_*275del	XP_011537023.1:n.*274_*275del
XM_011538722.1:c.*274_*275del	XP_011537024.1:n.*274_*275del
XM_017019919.1:c.*274_*275del	XP_016875408.1:n.*274_*275del
XM_024449179.1:c.*274_*275del	XP_024304947.1:n.*274_*275del
NM_003394.4:c.*274_*275del MANE Select	NP_003385.2:n.*274_*275del