Canonical Allele Identifier: CA2576520002
Gene: BCL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.63318820del , CM000680.2:g.63318820del GRCh38
NC_000018.9:g.60986053del , CM000680.1:g.60986053del GRCh37
NC_000018.8:g.59137033del NCBI36
NG_009361.1:g.5561del

Transcript Alleles

HGVS Amino-acid Change
ENST00000333681.5:c.-154del MANE Select ENSP00000329623.3:n.-154del
ENST00000333681.4:c.-154del ENSP00000329623.3:n.-154del
ENST00000398117.1:c.-154del ENSP00000381185.1:n.-154del
NM_000633.2:c.-154del NP_000624.2:n.-154del
NM_000657.2:c.-154del NP_000648.2:n.-154del
XM_011526135.1:c.-154del XP_011524437.1:n.-154del
XR_935246.1:n.959del
XR_935247.1:n.959del
XR_935248.1:n.738del
XM_011526135.3:c.-154del XP_011524437.1:n.-154del
XM_017025917.2:c.-154del XP_016881406.1:n.-154del
XR_935248.3:n.1240del
NM_000633.3:c.-154del MANE Select NP_000624.2:n.-154del
NM_000657.3:c.-154del NP_000648.2:n.-154del