Canonical Allele Identifier: CA2469911003
Gene: TBL1Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7003524_7003525delinsAG , CM000686.2:g.7003524_7003525delinsAG GRCh38
NC_000024.9:g.6871565_6871566delinsAG , CM000686.1:g.6871565_6871566delinsAG GRCh37
NC_000024.8:g.6931565_6931566delinsAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000383032.6:c.-140+7626_-140+7627delinsAG MANE Select ENSP00000372499.1:n.-140+7626_-140+7627delinsAG
ENST00000346432.3:c.-139-17925_-139-17924delinsAG ENSP00000328879.4:n.-139-17925_-139-17924delinsAG
ENST00000355162.6:c.-140+7626_-140+7627delinsAG ENSP00000347289.2:n.-140+7626_-140+7627delinsAG
ENST00000383032.5:c.-140+7626_-140+7627delinsAG ENSP00000372499.1:n.-140+7626_-140+7627delinsAG
NM_033284.1:c.-140+7626_-140+7627delinsAG NP_150600.1:n.-140+7626_-140+7627delinsAG
NM_134258.1:c.-140+7626_-140+7627delinsAG NP_599020.1:n.-140+7626_-140+7627delinsAG
NM_134259.1:c.-139-17925_-139-17924delinsAG NP_599021.1:n.-139-17925_-139-17924delinsAG
XM_017030086.1:c.-140+7626_-140+7627delinsAG XP_016885575.1:n.-140+7626_-140+7627delinsAG
XM_017030087.1:c.-140+7626_-140+7627delinsAG XP_016885576.1:n.-140+7626_-140+7627delinsAG
XM_024452497.1:c.-140+7626_-140+7627delinsAG XP_024308265.1:n.-140+7626_-140+7627delinsAG
NM_033284.2:c.-140+7626_-140+7627delinsAG MANE Select NP_150600.1:n.-140+7626_-140+7627delinsAG
NM_134258.2:c.-140+7626_-140+7627delinsAG NP_599020.1:n.-140+7626_-140+7627delinsAG
NM_134259.2:c.-139-17925_-139-17924delinsAG NP_599021.1:n.-139-17925_-139-17924delinsAG