Canonical Allele Identifier: CA1138865409
Gene: TBL1Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.6993191_6993192insCCTTTCTTTCTTTCTT , CM000686.2:g.6993191_6993192insCCTTTCTTTCTTTCTT GRCh38
NC_000024.9:g.6861232_6861233insCCTTTCTTTCTTTCTT , CM000686.1:g.6861232_6861233insCCTTTCTTTCTTTCTT GRCh37
NC_000024.8:g.6921232_6921233insCCTTTCTTTCTTTCTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000383032.6:c.-234-2613_-234-2612insCCTTTCTTTCTTTCTT MANE Select ENSP00000372499.1:n.-234-2613_-234-2612insCCTTTCTTTCTTTCTT
ENST00000346432.3:c.-140+14948_-140+14949insCCTTTCTTTCTTTCTT ENSP00000328879.4:n.-140+14948_-140+14949insCCTTTCTTTCTTTCTT
ENST00000355162.6:c.-234-2613_-234-2612insCCTTTCTTTCTTTCTT ENSP00000347289.2:n.-234-2613_-234-2612insCCTTTCTTTCTTTCTT
ENST00000383032.5:c.-234-2613_-234-2612insCCTTTCTTTCTTTCTT ENSP00000372499.1:n.-234-2613_-234-2612insCCTTTCTTTCTTTCTT
NM_033284.1:c.-234-2613_-234-2612insCCTTTCTTTCTTTCTT NP_150600.1:n.-234-2613_-234-2612insCCTTTCTTTCTTTCTT
NM_134258.1:c.-234-2613_-234-2612insCCTTTCTTTCTTTCTT NP_599020.1:n.-234-2613_-234-2612insCCTTTCTTTCTTTCTT
NM_134259.1:c.-140+14948_-140+14949insCCTTTCTTTCTTTCTT NP_599021.1:n.-140+14948_-140+14949insCCTTTCTTTCTTTCTT
XM_017030086.1:c.-234-2613_-234-2612insCCTTTCTTTCTTTCTT XP_016885575.1:n.-234-2613_-234-2612insCCTTTCTTTCTTTCTT
XM_017030087.1:c.-234-2613_-234-2612insCCTTTCTTTCTTTCTT XP_016885576.1:n.-234-2613_-234-2612insCCTTTCTTTCTTTCTT
XM_024452497.1:c.-234-2613_-234-2612insCCTTTCTTTCTTTCTT XP_024308265.1:n.-234-2613_-234-2612insCCTTTCTTTCTTTCTT
NM_033284.2:c.-234-2613_-234-2612insCCTTTCTTTCTTTCTT MANE Select NP_150600.1:n.-234-2613_-234-2612insCCTTTCTTTCTTTCTT
NM_134258.2:c.-234-2613_-234-2612insCCTTTCTTTCTTTCTT NP_599020.1:n.-234-2613_-234-2612insCCTTTCTTTCTTTCTT
NM_134259.2:c.-140+14948_-140+14949insCCTTTCTTTCTTTCTT NP_599021.1:n.-140+14948_-140+14949insCCTTTCTTTCTTTCTT