Canonical Allele Identifier: CA657488121

Gene: BCL2

Linked Data

• COSMIC: COSN23340075

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318785_63318786insG , CM000680.2:g.63318785_63318786insG	GRCh38
NC_000018.9:g.60986018_60986019insG , CM000680.1:g.60986018_60986019insG	GRCh37
NC_000018.8:g.59136998_59136999insG	NCBI36
NG_009361.1:g.5595_5596insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-120_-119insC MANE Select	ENSP00000329623.3:n.-120_-119insC
ENST00000333681.4:c.-120_-119insC	ENSP00000329623.3:n.-120_-119insC
ENST00000398117.1:c.-120_-119insC	ENSP00000381185.1:n.-120_-119insC
ENST00000589955.2:c.-120_-119insC	ENSP00000466417.1:n.-120_-119insC
NM_000633.2:c.-120_-119insC	NP_000624.2:n.-120_-119insC
NM_000657.2:c.-120_-119insC	NP_000648.2:n.-120_-119insC
XM_011526135.1:c.-120_-119insC	XP_011524437.1:n.-120_-119insC
XR_935246.1:n.993_994insC
XR_935247.1:n.993_994insC
XR_935248.1:n.772_773insC
XM_011526135.3:c.-120_-119insC	XP_011524437.1:n.-120_-119insC
XM_017025917.2:c.-120_-119insC	XP_016881406.1:n.-120_-119insC
XR_935248.3:n.1274_1275insC
NM_000633.3:c.-120_-119insC MANE Select	NP_000624.2:n.-120_-119insC
NM_000657.3:c.-120_-119insC	NP_000648.2:n.-120_-119insC