Canonical Allele Identifier: CA2509882330
Gene: TBL1Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.6920233del , CM000686.2:g.6920233del GRCh38
NC_000024.9:g.6788274del , CM000686.1:g.6788274del GRCh37
NC_000024.8:g.6848274del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000383032.6:c.-266+8061del MANE Select ENSP00000372499.1:n.-266+8061del
ENST00000346432.3:c.-171+8061del ENSP00000328879.4:n.-171+8061del
ENST00000355162.6:c.-235+8061del ENSP00000347289.2:n.-235+8061del
ENST00000383032.5:c.-266+8061del ENSP00000372499.1:n.-266+8061del
NM_033284.1:c.-266+8061del NP_150600.1:n.-266+8061del
NM_134258.1:c.-235+8061del NP_599020.1:n.-235+8061del
NM_134259.1:c.-171+8061del NP_599021.1:n.-171+8061del
XM_017030086.1:c.-266+8061del XP_016885575.1:n.-266+8061del
XM_017030087.1:c.-266+8061del XP_016885576.1:n.-266+8061del
XM_024452497.1:c.-266+8061del XP_024308265.1:n.-266+8061del
NM_033284.2:c.-266+8061del MANE Select NP_150600.1:n.-266+8061del
NM_134258.2:c.-235+8061del NP_599020.1:n.-235+8061del
NM_134259.2:c.-171+8061del NP_599021.1:n.-171+8061del