Canonical Allele Identifier: CA2469912366
Gene: TBL1Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7031695A= , CM000686.2:g.7031695A= GRCh38
NC_000024.9:g.6899736A= , CM000686.1:g.6899736A= GRCh37
NC_000024.8:g.6959736A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000383032.6:c.58+6553A= MANE Select ENSP00000372499.1:n.58+6553A=
ENST00000346432.3:c.58+6553A= ENSP00000328879.4:n.58+6553A=
ENST00000355162.6:c.58+6553A= ENSP00000347289.2:n.58+6553A=
ENST00000383032.5:c.58+6553A= ENSP00000372499.1:n.58+6553A=
NM_033284.1:c.58+6553A= NP_150600.1:n.58+6553A=
NM_134258.1:c.58+6553A= NP_599020.1:n.58+6553A=
NM_134259.1:c.58+6553A= NP_599021.1:n.58+6553A=
XM_017030086.1:c.58+6553A= XP_016885575.1:n.58+6553A=
XM_017030087.1:c.58+6553A= XP_016885576.1:n.58+6553A=
XM_024452497.1:c.58+6553A= XP_024308265.1:n.58+6553A=
NM_033284.2:c.58+6553A= MANE Select NP_150600.1:n.58+6553A=
NM_134258.2:c.58+6553A= NP_599020.1:n.58+6553A=
NM_134259.2:c.58+6553A= NP_599021.1:n.58+6553A=