Canonical Allele Identifier: CA2469910302
Gene: TBL1Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.6991637C= , CM000686.2:g.6991637C= GRCh38
NC_000024.9:g.6859678C= , CM000686.1:g.6859678C= GRCh37
NC_000024.8:g.6919678C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000383032.6:c.-234-4167C= MANE Select ENSP00000372499.1:n.-234-4167C=
ENST00000346432.3:c.-140+13394C= ENSP00000328879.4:n.-140+13394C=
ENST00000355162.6:c.-234-4167C= ENSP00000347289.2:n.-234-4167C=
ENST00000383032.5:c.-234-4167C= ENSP00000372499.1:n.-234-4167C=
NM_033284.1:c.-234-4167C= NP_150600.1:n.-234-4167C=
NM_134258.1:c.-234-4167C= NP_599020.1:n.-234-4167C=
NM_134259.1:c.-140+13394C= NP_599021.1:n.-140+13394C=
XM_017030086.1:c.-234-4167C= XP_016885575.1:n.-234-4167C=
XM_017030087.1:c.-234-4167C= XP_016885576.1:n.-234-4167C=
XM_024452497.1:c.-234-4167C= XP_024308265.1:n.-234-4167C=
NM_033284.2:c.-234-4167C= MANE Select NP_150600.1:n.-234-4167C=
NM_134258.2:c.-234-4167C= NP_599020.1:n.-234-4167C=
NM_134259.2:c.-140+13394C= NP_599021.1:n.-140+13394C=