Canonical Allele Identifier: CA384683668

Gene: WNT10B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48970477A>T , CM000674.2:g.48970477A>T	GRCh38
NC_000012.11:g.49364260A>T , CM000674.1:g.49364260A>T	GRCh37
NC_000012.10:g.47650527A>T	NCBI36
NG_023347.1:g.6382T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003394.4:c.53T>A MANE Select	NP_003385.2:p.Leu18Gln
ENST00000301061.9:c.53T>A MANE Select	ENSP00000301061.4:p.Leu18Gln
NM_003394.3:c.53T>A	NP_003385.2:p.Leu18Gln
ENST00000301061.8:c.53T>A	ENSP00000301061.4:p.Leu18Gln
ENST00000403957.5:c.53T>A	ENSP00000385980.1:p.Leu18Gln
ENST00000407467.5:c.53T>A	ENSP00000384691.1:p.Leu18Gln
ENST00000413630.1:c.53T>A	ENSP00000398473.1:p.Leu18Gln
ENST00000420388.1:c.53T>A	ENSP00000404896.1:p.Leu18Gln
ENST00000475740.1:n.176T>A
XM_011538721.1:c.-349T>A	XP_011537023.1:n.-349T>A
XM_011538723.1:c.53T>A	XP_011537025.1:p.Leu18Gln
XM_011538724.1:c.53T>A	XP_011537026.1:p.Leu18Gln
XM_024449179.1:c.-349T>A	XP_024304947.1:n.-349T>A