Canonical Allele Identifier: CA1946977089
Gene: BET1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.202955_202958delinsATTT , CM000673.2:g.202955_202958delinsATTT GRCh38
NC_000011.9:g.202955_202958delinsATTT , CM000673.1:g.202955_202958delinsATTT GRCh37
NC_000011.8:g.192955_192958delinsATTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000382762.8:c.*2344_*2347delinsAAAT MANE Select ENSP00000372210.3:n.*2344_*2347delinsAAAT
ENST00000325147.13:c.*2512_*2515delinsAAAT ENSP00000339093.7:n.*2512_*2515delinsAAAT
ENST00000382762.7:c.*2344_*2347delinsAAAT ENSP00000372210.3:n.*2344_*2347delinsAAAT
ENST00000410108.5:c.168+2653_168+2656delinsAAAT ENSP00000386558.1:n.168+2653_168+2656delinsAAAT
NM_001098787.1:c.*2344_*2347delinsAAAT NP_001092257.1:n.*2344_*2347delinsAAAT
NM_016526.4:c.*2512_*2515delinsAAAT NP_057610.2:n.*2512_*2515delinsAAAT
NM_001098787.2:c.*2344_*2347delinsAAAT MANE Select NP_001092257.1:n.*2344_*2347delinsAAAT
NM_016526.5:c.*2512_*2515delinsAAAT NP_057610.2:n.*2512_*2515delinsAAAT