Canonical Allele Identifier: CA118933

Gene: WNT10B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48966271G>A , CM000674.2:g.48966271G>A	GRCh38
NC_000012.11:g.49360054G>A , CM000674.1:g.49360054G>A	GRCh37
NC_000012.10:g.47646321G>A	NCBI36
NG_023347.1:g.10588C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003394.4:c.994C>T MANE Select	NP_003385.2:p.Arg332Trp
ENST00000301061.9:c.994C>T MANE Select	ENSP00000301061.4:p.Arg332Trp
NM_003394.3:c.994C>T	NP_003385.2:p.Arg332Trp
ENST00000301061.8:c.994C>T	ENSP00000301061.4:p.Arg332Trp
ENST00000403957.5:c.*276C>T	ENSP00000385980.1:n.*276C>T
ENST00000407467.5:c.*276C>T	ENSP00000384691.1:n.*276C>T
XM_011538721.1:c.628C>T	XP_011537023.1:p.Arg210Trp
XM_011538722.1:c.628C>T	XP_011537024.1:p.Arg210Trp
XM_011538724.1:c.*272C>T	XP_011537026.1:n.*272C>T
XM_017019919.1:c.628C>T	XP_016875408.1:p.Arg210Trp
XM_024449179.1:c.628C>T	XP_024304947.1:p.Arg210Trp