Canonical Allele Identifier: CA384681435

Gene: WNT10B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48970169T>G , CM000674.2:g.48970169T>G	GRCh38
NC_000012.11:g.49363952T>G , CM000674.1:g.49363952T>G	GRCh37
NC_000012.10:g.47650219T>G	NCBI36
NG_023347.1:g.6690A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_003394.4:c.257A>C MANE Select	NP_003385.2:p.Gln86Pro
ENST00000301061.9:c.257A>C MANE Select	ENSP00000301061.4:p.Gln86Pro
NM_003394.3:c.257A>C	NP_003385.2:p.Gln86Pro
ENST00000301061.8:c.257A>C	ENSP00000301061.4:p.Gln86Pro
ENST00000403957.5:c.257A>C	ENSP00000385980.1:p.Gln86Pro
ENST00000407467.5:c.257A>C	ENSP00000384691.1:p.Gln86Pro
ENST00000413630.1:c.257A>C	ENSP00000398473.1:p.Gln86Pro
ENST00000420388.1:c.257A>C	ENSP00000404896.1:p.Gln86Pro
ENST00000475740.1:n.380A>C
XM_011538721.1:c.-145A>C	XP_011537023.1:n.-145A>C
XM_011538722.1:c.-200A>C	XP_011537024.1:n.-200A>C
XM_011538723.1:c.257A>C	XP_011537025.1:p.Gln86Pro
XM_011538724.1:c.257A>C	XP_011537026.1:p.Gln86Pro
XM_024449179.1:c.-145A>C	XP_024304947.1:n.-145A>C