Canonical Allele Identifier: CA2469910304
Gene: TBL1Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.6991650T= , CM000686.2:g.6991650T= GRCh38
NC_000024.9:g.6859691T= , CM000686.1:g.6859691T= GRCh37
NC_000024.8:g.6919691T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000383032.6:c.-234-4154T= MANE Select ENSP00000372499.1:n.-234-4154T=
ENST00000346432.3:c.-140+13407T= ENSP00000328879.4:n.-140+13407T=
ENST00000355162.6:c.-234-4154T= ENSP00000347289.2:n.-234-4154T=
ENST00000383032.5:c.-234-4154T= ENSP00000372499.1:n.-234-4154T=
NM_033284.1:c.-234-4154T= NP_150600.1:n.-234-4154T=
NM_134258.1:c.-234-4154T= NP_599020.1:n.-234-4154T=
NM_134259.1:c.-140+13407T= NP_599021.1:n.-140+13407T=
XM_017030086.1:c.-234-4154T= XP_016885575.1:n.-234-4154T=
XM_017030087.1:c.-234-4154T= XP_016885576.1:n.-234-4154T=
XM_024452497.1:c.-234-4154T= XP_024308265.1:n.-234-4154T=
NM_033284.2:c.-234-4154T= MANE Select NP_150600.1:n.-234-4154T=
NM_134258.2:c.-234-4154T= NP_599020.1:n.-234-4154T=
NM_134259.2:c.-140+13407T= NP_599021.1:n.-140+13407T=