Canonical Allele Identifier: CA2565096766

Gene: WNT10B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48965824_48965825insTCCCTATA , CM000674.2:g.48965824_48965825insTCCCTATA	GRCh38
NC_000012.11:g.49359607_49359608insTCCCTATA , CM000674.1:g.49359607_49359608insTCCCTATA	GRCh37
NC_000012.10:g.47645874_47645875insTCCCTATA	NCBI36
NG_023347.1:g.11034_11035insTATAGGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301061.9:c.*270_*271insTATAGGGA MANE Select	ENSP00000301061.4:n.*270_*271insTATAGGGA
ENST00000301061.8:c.*270_*271insTATAGGGA	ENSP00000301061.4:n.*270_*271insTATAGGGA
ENST00000403957.5:c.*722_*723insTATAGGGA	ENSP00000385980.1:n.*722_*723insTATAGGGA
ENST00000407467.5:c.*722_*723insTATAGGGA	ENSP00000384691.1:n.*722_*723insTATAGGGA
NM_003394.3:c.*270_*271insTATAGGGA	NP_003385.2:n.*270_*271insTATAGGGA
XM_011538721.1:c.*270_*271insTATAGGGA	XP_011537023.1:n.*270_*271insTATAGGGA
XM_011538722.1:c.*270_*271insTATAGGGA	XP_011537024.1:n.*270_*271insTATAGGGA
XM_017019919.1:c.*270_*271insTATAGGGA	XP_016875408.1:n.*270_*271insTATAGGGA
XM_024449179.1:c.*270_*271insTATAGGGA	XP_024304947.1:n.*270_*271insTATAGGGA
NM_003394.4:c.*270_*271insTATAGGGA MANE Select	NP_003385.2:n.*270_*271insTATAGGGA