Canonical Allele Identifier: CA657488382

Gene: BCL2

Linked Data

• COSMIC: COSN25234291

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318907del , CM000680.2:g.63318907del	GRCh38
NC_000018.9:g.60986140del , CM000680.1:g.60986140del	GRCh37
NC_000018.8:g.59137120del	NCBI36
NG_009361.1:g.5475del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-240del MANE Select	ENSP00000329623.3:n.-240del
ENST00000333681.4:c.-240del	ENSP00000329623.3:n.-240del
ENST00000398117.1:c.-240del	ENSP00000381185.1:n.-240del
NM_000633.2:c.-240del	NP_000624.2:n.-240del
NM_000657.2:c.-240del	NP_000648.2:n.-240del
XM_011526135.1:c.-240del	XP_011524437.1:n.-240del
XR_935246.1:n.873del
XR_935247.1:n.873del
XR_935248.1:n.652del
XM_011526135.3:c.-240del	XP_011524437.1:n.-240del
XM_017025917.2:c.-240del	XP_016881406.1:n.-240del
XR_935248.3:n.1154del
NM_000633.3:c.-240del MANE Select	NP_000624.2:n.-240del
NM_000657.3:c.-240del	NP_000648.2:n.-240del