Canonical Allele Identifier: CA1946977094
Gene: BET1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.202961_202964delinsATTG , CM000673.2:g.202961_202964delinsATTG GRCh38
NC_000011.9:g.202961_202964delinsATTG , CM000673.1:g.202961_202964delinsATTG GRCh37
NC_000011.8:g.192961_192964delinsATTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000382762.8:c.*2338_*2341delinsCAAT MANE Select ENSP00000372210.3:n.*2338_*2341delinsCAAT
ENST00000325147.13:c.*2506_*2509delinsCAAT ENSP00000339093.7:n.*2506_*2509delinsCAAT
ENST00000382762.7:c.*2338_*2341delinsCAAT ENSP00000372210.3:n.*2338_*2341delinsCAAT
ENST00000410108.5:c.168+2647_168+2650delinsCAAT ENSP00000386558.1:n.168+2647_168+2650delinsCAAT
NM_001098787.1:c.*2338_*2341delinsCAAT NP_001092257.1:n.*2338_*2341delinsCAAT
NM_016526.4:c.*2506_*2509delinsCAAT NP_057610.2:n.*2506_*2509delinsCAAT
NM_001098787.2:c.*2338_*2341delinsCAAT MANE Select NP_001092257.1:n.*2338_*2341delinsCAAT
NM_016526.5:c.*2506_*2509delinsCAAT NP_057610.2:n.*2506_*2509delinsCAAT