Canonical Allele Identifier: CA657488571

Gene: BCL2

Linked Data

• COSMIC: COSN23077921

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318926_63318927insG , CM000680.2:g.63318926_63318927insG	GRCh38
NC_000018.9:g.60986159_60986160insG , CM000680.1:g.60986159_60986160insG	GRCh37
NC_000018.8:g.59137139_59137140insG	NCBI36
NG_009361.1:g.5454_5455insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-261_-260insC MANE Select	ENSP00000329623.3:n.-261_-260insC
ENST00000333681.4:c.-261_-260insC	ENSP00000329623.3:n.-261_-260insC
ENST00000398117.1:c.-261_-260insC	ENSP00000381185.1:n.-261_-260insC
NM_000633.2:c.-261_-260insC	NP_000624.2:n.-261_-260insC
NM_000657.2:c.-261_-260insC	NP_000648.2:n.-261_-260insC
XM_011526135.1:c.-261_-260insC	XP_011524437.1:n.-261_-260insC
XR_935246.1:n.852_853insC
XR_935247.1:n.852_853insC
XR_935248.1:n.631_632insC
XM_011526135.3:c.-261_-260insC	XP_011524437.1:n.-261_-260insC
XM_017025917.2:c.-261_-260insC	XP_016881406.1:n.-261_-260insC
XR_935248.3:n.1133_1134insC
NM_000633.3:c.-261_-260insC MANE Select	NP_000624.2:n.-261_-260insC
NM_000657.3:c.-261_-260insC	NP_000648.2:n.-261_-260insC