Canonical Allele Identifier: CA6544127

Gene: WNT10B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48967981G>A , CM000674.2:g.48967981G>A	GRCh38
NC_000012.11:g.49361764G>A , CM000674.1:g.49361764G>A	GRCh37
NC_000012.10:g.47648031G>A	NCBI36
NG_023347.1:g.8878C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003394.4:c.676C>T MANE Select	NP_003385.2:p.Arg226Ter
ENST00000301061.9:c.676C>T MANE Select	ENSP00000301061.4:p.Arg226Ter
NM_003394.3:c.676C>T	NP_003385.2:p.Arg226Ter
ENST00000301061.8:c.676C>T	ENSP00000301061.4:p.Arg226Ter
ENST00000403957.5:c.480C>T	ENSP00000385980.1:p.His160=
ENST00000407467.5:c.534C>T	ENSP00000384691.1:p.His178=
XM_011538721.1:c.310C>T	XP_011537023.1:p.Arg104Ter
XM_011538722.1:c.310C>T	XP_011537024.1:p.Arg104Ter
XM_011538723.1:c.534C>T	XP_011537025.1:p.His178=
XM_011538724.1:c.449C>T	XP_011537026.1:p.Thr150Met
XM_017019919.1:c.310C>T	XP_016875408.1:p.Arg104Ter
XM_024449179.1:c.310C>T	XP_024304947.1:p.Arg104Ter