Canonical Allele Identifier: CA2262422426
Gene: WNT9B HGNC NCBI
LRRC37A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46871631_46871634delinsGAGA , CM000679.2:g.46871631_46871634delinsGAGA GRCh38
NC_000017.10:g.44948997_44949000delinsGAGA , CM000679.1:g.44948997_44949000delinsGAGA GRCh37
NC_000017.9:g.42303996_42303999delinsGAGA NCBI36
NG_029164.1:g.25030_25033delinsGAGA
NG_029164.3:g.25030_25033delinsGAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000290015.7:c.78-886_78-883delinsGAGA (WNT9B) MANE Select ENSP00000290015.2:n.78-886_78-883delinsGAGA
ENST00000290015.6:c.78-886_78-883delinsGAGA (WNT9B) ENSP00000290015.2:n.78-886_78-883delinsGAGA
ENST00000393461.2:c.78-886_78-883delinsGAGA (WNT9B) ENSP00000377105.2:n.78-886_78-883delinsGAGA
ENST00000575372.5:c.96-886_96-883delinsGAGA (WNT9B) ENSP00000458192.1:n.96-886_96-883delinsGAGA
NM_003396.1:c.78-886_78-883delinsGAGA (WNT9B) NP_003387.1:n.78-886_78-883delinsGAGA
XM_005257637.2:c.78-886_78-883delinsGAGA (WNT9B) XP_005257694.1:n.78-886_78-883delinsGAGA
XM_011525178.1:c.96-886_96-883delinsGAGA (WNT9B) XP_011523480.1:n.96-886_96-883delinsGAGA
NM_001320458.1:c.78-886_78-883delinsGAGA (WNT9B) NP_001307387.1:n.78-886_78-883delinsGAGA
NM_003396.2:c.78-886_78-883delinsGAGA (WNT9B) NP_003387.1:n.78-886_78-883delinsGAGA
XM_011525178.2:c.96-886_96-883delinsGAGA (WNT9B) XP_011523480.1:n.96-886_96-883delinsGAGA
XM_024450773.1:c.4810-177425_4810-177422delinsGAGA (LRRC37A2) XP_024306541.1:n.4810-177425_4810-177422delinsGAGA
NM_003396.3:c.78-886_78-883delinsGAGA (WNT9B) MANE Select NP_003387.1:n.78-886_78-883delinsGAGA
NM_001320458.2:c.78-886_78-883delinsGAGA (WNT9B) NP_001307387.1:n.78-886_78-883delinsGAGA