Canonical Allele Identifier: CA2824507850
Gene: TBL1Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7083902_7083903del , CM000686.2:g.7083902_7083903del GRCh38
NC_000024.9:g.6951943_6951944del , CM000686.1:g.6951943_6951944del GRCh37
NC_000024.8:g.7011943_7011944del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000383032.6:c.1078-1996_1078-1995del MANE Select ENSP00000372499.1:n.1078-1996_1078-1995del
ENST00000346432.3:c.1078-1996_1078-1995del ENSP00000328879.4:n.1078-1996_1078-1995del
ENST00000355162.6:c.1078-1996_1078-1995del ENSP00000347289.2:n.1078-1996_1078-1995del
ENST00000383032.5:c.1078-1996_1078-1995del ENSP00000372499.1:n.1078-1996_1078-1995del
NM_033284.1:c.1078-1996_1078-1995del NP_150600.1:n.1078-1996_1078-1995del
NM_134258.1:c.1078-1996_1078-1995del NP_599020.1:n.1078-1996_1078-1995del
NM_134259.1:c.1078-1996_1078-1995del NP_599021.1:n.1078-1996_1078-1995del
XM_005262572.2:c.1120-1996_1120-1995del XP_005262629.1:n.1120-1996_1120-1995del
XM_005262572.3:c.1120-1996_1120-1995del XP_005262629.1:n.1120-1996_1120-1995del
XM_017030086.1:c.1078-1996_1078-1995del XP_016885575.1:n.1078-1996_1078-1995del
XM_017030087.1:c.1078-1996_1078-1995del XP_016885576.1:n.1078-1996_1078-1995del
XM_024452497.1:c.1078-1996_1078-1995del XP_024308265.1:n.1078-1996_1078-1995del
NM_033284.2:c.1078-1996_1078-1995del MANE Select NP_150600.1:n.1078-1996_1078-1995del
NM_134258.2:c.1078-1996_1078-1995del NP_599020.1:n.1078-1996_1078-1995del
NM_134259.2:c.1078-1996_1078-1995del NP_599021.1:n.1078-1996_1078-1995del