Canonical Allele Identifier: CA657488248

Gene: BCL2

Linked Data

• COSMIC: COSN23379104

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318874_63318875insC , CM000680.2:g.63318874_63318875insC	GRCh38
NC_000018.9:g.60986107_60986108insC , CM000680.1:g.60986107_60986108insC	GRCh37
NC_000018.8:g.59137087_59137088insC	NCBI36
NG_009361.1:g.5506_5507insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-209_-208insG MANE Select	ENSP00000329623.3:n.-209_-208insG
ENST00000333681.4:c.-209_-208insG	ENSP00000329623.3:n.-209_-208insG
ENST00000398117.1:c.-209_-208insG	ENSP00000381185.1:n.-209_-208insG
NM_000633.2:c.-209_-208insG	NP_000624.2:n.-209_-208insG
NM_000657.2:c.-209_-208insG	NP_000648.2:n.-209_-208insG
XM_011526135.1:c.-209_-208insG	XP_011524437.1:n.-209_-208insG
XR_935246.1:n.904_905insG
XR_935247.1:n.904_905insG
XR_935248.1:n.683_684insG
XM_011526135.3:c.-209_-208insG	XP_011524437.1:n.-209_-208insG
XM_017025917.2:c.-209_-208insG	XP_016881406.1:n.-209_-208insG
XR_935248.3:n.1185_1186insG
NM_000633.3:c.-209_-208insG MANE Select	NP_000624.2:n.-209_-208insG
NM_000657.3:c.-209_-208insG	NP_000648.2:n.-209_-208insG