Canonical Allele Identifier: CA657488590

Gene: BCL2

Linked Data

• COSMIC: COSN23176077 ; COSN23274377

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318930_63318931insG , CM000680.2:g.63318930_63318931insG	GRCh38
NC_000018.9:g.60986163_60986164insG , CM000680.1:g.60986163_60986164insG	GRCh37
NC_000018.8:g.59137143_59137144insG	NCBI36
NG_009361.1:g.5450_5451insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-265_-264insC MANE Select	ENSP00000329623.3:n.-265_-264insC
ENST00000333681.4:c.-265_-264insC	ENSP00000329623.3:n.-265_-264insC
ENST00000398117.1:c.-265_-264insC	ENSP00000381185.1:n.-265_-264insC
NM_000633.2:c.-265_-264insC	NP_000624.2:n.-265_-264insC
NM_000657.2:c.-265_-264insC	NP_000648.2:n.-265_-264insC
XM_011526135.1:c.-265_-264insC	XP_011524437.1:n.-265_-264insC
XR_935246.1:n.848_849insC
XR_935247.1:n.848_849insC
XR_935248.1:n.627_628insC
XM_011526135.3:c.-265_-264insC	XP_011524437.1:n.-265_-264insC
XM_017025917.2:c.-265_-264insC	XP_016881406.1:n.-265_-264insC
XR_935248.3:n.1129_1130insC
NM_000633.3:c.-265_-264insC MANE Select	NP_000624.2:n.-265_-264insC
NM_000657.3:c.-265_-264insC	NP_000648.2:n.-265_-264insC