Canonical Allele Identifier: CA1946977103
Gene: BET1L HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.202981T= , CM000673.2:g.202981T= GRCh38
NC_000011.9:g.202981T= , CM000673.1:g.202981T= GRCh37
NC_000011.8:g.192981T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000382762.8:c.*2321A= MANE Select ENSP00000372210.3:n.*2321A=
ENST00000325147.13:c.*2489A= ENSP00000339093.7:n.*2489A=
ENST00000382762.7:c.*2321A= ENSP00000372210.3:n.*2321A=
ENST00000410108.5:c.168+2630A= ENSP00000386558.1:n.168+2630A=
NM_001098787.1:c.*2321A= NP_001092257.1:n.*2321A=
NM_016526.4:c.*2489A= NP_057610.2:n.*2489A=
NM_001098787.2:c.*2321A= MANE Select NP_001092257.1:n.*2321A=
NM_016526.5:c.*2489A= NP_057610.2:n.*2489A=
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