Canonical Allele Identifier: CA2824505565
Gene: TBL1Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.6993057_6993063del , CM000686.2:g.6993057_6993063del GRCh38
NC_000024.9:g.6861098_6861104del , CM000686.1:g.6861098_6861104del GRCh37
NC_000024.8:g.6921098_6921104del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000383032.6:c.-234-2747_-234-2741del MANE Select ENSP00000372499.1:n.-234-2747_-234-2741del
ENST00000346432.3:c.-140+14814_-140+14820del ENSP00000328879.4:n.-140+14814_-140+14820del
ENST00000355162.6:c.-234-2747_-234-2741del ENSP00000347289.2:n.-234-2747_-234-2741del
ENST00000383032.5:c.-234-2747_-234-2741del ENSP00000372499.1:n.-234-2747_-234-2741del
NM_033284.1:c.-234-2747_-234-2741del NP_150600.1:n.-234-2747_-234-2741del
NM_134258.1:c.-234-2747_-234-2741del NP_599020.1:n.-234-2747_-234-2741del
NM_134259.1:c.-140+14814_-140+14820del NP_599021.1:n.-140+14814_-140+14820del
XM_017030086.1:c.-234-2747_-234-2741del XP_016885575.1:n.-234-2747_-234-2741del
XM_017030087.1:c.-234-2747_-234-2741del XP_016885576.1:n.-234-2747_-234-2741del
XM_024452497.1:c.-234-2747_-234-2741del XP_024308265.1:n.-234-2747_-234-2741del
NM_033284.2:c.-234-2747_-234-2741del MANE Select NP_150600.1:n.-234-2747_-234-2741del
NM_134258.2:c.-234-2747_-234-2741del NP_599020.1:n.-234-2747_-234-2741del
NM_134259.2:c.-140+14814_-140+14820del NP_599021.1:n.-140+14814_-140+14820del