Canonical Allele Identifier: CA2469910419
Gene: TBL1Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.6993190_6993193delinsTTTC , CM000686.2:g.6993190_6993193delinsTTTC GRCh38
NC_000024.9:g.6861231_6861234delinsTTTC , CM000686.1:g.6861231_6861234delinsTTTC GRCh37
NC_000024.8:g.6921231_6921234delinsTTTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000383032.6:c.-234-2614_-234-2611delinsTTTC MANE Select ENSP00000372499.1:n.-234-2614_-234-2611delinsTTTC
ENST00000346432.3:c.-140+14947_-140+14950delinsTTTC ENSP00000328879.4:n.-140+14947_-140+14950delinsTTTC
ENST00000355162.6:c.-234-2614_-234-2611delinsTTTC ENSP00000347289.2:n.-234-2614_-234-2611delinsTTTC
ENST00000383032.5:c.-234-2614_-234-2611delinsTTTC ENSP00000372499.1:n.-234-2614_-234-2611delinsTTTC
NM_033284.1:c.-234-2614_-234-2611delinsTTTC NP_150600.1:n.-234-2614_-234-2611delinsTTTC
NM_134258.1:c.-234-2614_-234-2611delinsTTTC NP_599020.1:n.-234-2614_-234-2611delinsTTTC
NM_134259.1:c.-140+14947_-140+14950delinsTTTC NP_599021.1:n.-140+14947_-140+14950delinsTTTC
XM_017030086.1:c.-234-2614_-234-2611delinsTTTC XP_016885575.1:n.-234-2614_-234-2611delinsTTTC
XM_017030087.1:c.-234-2614_-234-2611delinsTTTC XP_016885576.1:n.-234-2614_-234-2611delinsTTTC
XM_024452497.1:c.-234-2614_-234-2611delinsTTTC XP_024308265.1:n.-234-2614_-234-2611delinsTTTC
NM_033284.2:c.-234-2614_-234-2611delinsTTTC MANE Select NP_150600.1:n.-234-2614_-234-2611delinsTTTC
NM_134258.2:c.-234-2614_-234-2611delinsTTTC NP_599020.1:n.-234-2614_-234-2611delinsTTTC
NM_134259.2:c.-140+14947_-140+14950delinsTTTC NP_599021.1:n.-140+14947_-140+14950delinsTTTC