Canonical Allele Identifier: CA2642093038
Gene: BCL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.63318907_63318916del , CM000680.2:g.63318907_63318916del GRCh38
NC_000018.9:g.60986140_60986149del , CM000680.1:g.60986140_60986149del GRCh37
NC_000018.8:g.59137120_59137129del NCBI36
NG_009361.1:g.5467_5476del

Transcript Alleles

HGVS Amino-acid Change
ENST00000333681.5:c.-248_-239del MANE Select ENSP00000329623.3:n.-248_-239del
ENST00000333681.4:c.-248_-239del ENSP00000329623.3:n.-248_-239del
ENST00000398117.1:c.-248_-239del ENSP00000381185.1:n.-248_-239del
NM_000633.2:c.-248_-239del NP_000624.2:n.-248_-239del
NM_000657.2:c.-248_-239del NP_000648.2:n.-248_-239del
XM_011526135.1:c.-248_-239del XP_011524437.1:n.-248_-239del
XR_935246.1:n.865_874del
XR_935247.1:n.865_874del
XR_935248.1:n.644_653del
XM_011526135.3:c.-248_-239del XP_011524437.1:n.-248_-239del
XM_017025917.2:c.-248_-239del XP_016881406.1:n.-248_-239del
XR_935248.3:n.1146_1155del
NM_000633.3:c.-248_-239del MANE Select NP_000624.2:n.-248_-239del
NM_000657.3:c.-248_-239del NP_000648.2:n.-248_-239del