Canonical Allele Identifier: CA2618595982

Gene: WNT10B

Linked Data

• gnomAD v4: 12-48965946-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48965947dup , CM000674.2:g.48965947dup	GRCh38
NC_000012.11:g.49359730dup , CM000674.1:g.49359730dup	GRCh37
NC_000012.10:g.47645997dup	NCBI36
NG_023347.1:g.10912dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301061.9:c.*148dup MANE Select	ENSP00000301061.4:n.*148dup
ENST00000301061.8:c.*148dup	ENSP00000301061.4:n.*148dup
ENST00000403957.5:c.*600dup	ENSP00000385980.1:n.*600dup
ENST00000407467.5:c.*600dup	ENSP00000384691.1:n.*600dup
NM_003394.3:c.*148dup	NP_003385.2:n.*148dup
XM_011538721.1:c.*148dup	XP_011537023.1:n.*148dup
XM_011538722.1:c.*148dup	XP_011537024.1:n.*148dup
XM_017019919.1:c.*148dup	XP_016875408.1:n.*148dup
XM_024449179.1:c.*148dup	XP_024304947.1:n.*148dup
NM_003394.4:c.*148dup MANE Select	NP_003385.2:n.*148dup