Canonical Allele Identifier: CA2575143609

Gene: WNT10B

Linked Data

• gnomAD v4: 12-48966202-CGTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48966205_48966207del , CM000674.2:g.48966205_48966207del	GRCh38
NC_000012.11:g.49359988_49359990del , CM000674.1:g.49359988_49359990del	GRCh37
NC_000012.10:g.47646255_47646257del	NCBI36
NG_023347.1:g.10654_10656del

Transcript Alleles

HGVS	Amino-acid change
ENST00000301061.9:c.1060_1062del MANE Select	ENSP00000301061.4:p.Asn354del
ENST00000301061.8:c.1060_1062del	ENSP00000301061.4:p.Asn354del
ENST00000403957.5:c.*342_*344del	ENSP00000385980.1:n.*342_*344del
ENST00000407467.5:c.*342_*344del	ENSP00000384691.1:n.*342_*344del
NM_003394.3:c.1060_1062del	NP_003385.2:p.Asn354del
XM_011538721.1:c.694_696del	XP_011537023.1:p.Asn232del
XM_011538722.1:c.694_696del	XP_011537024.1:p.Asn232del
XM_011538724.1:c.*338_*340del	XP_011537026.1:n.*338_*340del
XM_017019919.1:c.694_696del	XP_016875408.1:p.Asn232del
XM_024449179.1:c.694_696del	XP_024304947.1:p.Asn232del
NM_003394.4:c.1060_1062del MANE Select	NP_003385.2:p.Asn354del