Canonical Allele Identifier: CA2618596063

Gene: WNT10B

Linked Data

• gnomAD v4: 12-48966030-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48966033del , CM000674.2:g.48966033del	GRCh38
NC_000012.11:g.49359816del , CM000674.1:g.49359816del	GRCh37
NC_000012.10:g.47646083del	NCBI36
NG_023347.1:g.10828del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301061.9:c.*64del MANE Select	ENSP00000301061.4:n.*64del
ENST00000301061.8:c.*64del	ENSP00000301061.4:n.*64del
ENST00000403957.5:c.*516del	ENSP00000385980.1:n.*516del
ENST00000407467.5:c.*516del	ENSP00000384691.1:n.*516del
NM_003394.3:c.*64del	NP_003385.2:n.*64del
XM_011538721.1:c.*64del	XP_011537023.1:n.*64del
XM_011538722.1:c.*64del	XP_011537024.1:n.*64del
XM_017019919.1:c.*64del	XP_016875408.1:n.*64del
XM_024449179.1:c.*64del	XP_024304947.1:n.*64del
NM_003394.4:c.*64del MANE Select	NP_003385.2:n.*64del