Canonical Allele Identifier: CA657488413

Gene: BCL2

Linked Data

• COSMIC: COSN23277148

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318909_63318910insC , CM000680.2:g.63318909_63318910insC	GRCh38
NC_000018.9:g.60986142_60986143insC , CM000680.1:g.60986142_60986143insC	GRCh37
NC_000018.8:g.59137122_59137123insC	NCBI36
NG_009361.1:g.5471_5472insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-244_-243insG MANE Select	ENSP00000329623.3:n.-244_-243insG
ENST00000333681.4:c.-244_-243insG	ENSP00000329623.3:n.-244_-243insG
ENST00000398117.1:c.-244_-243insG	ENSP00000381185.1:n.-244_-243insG
NM_000633.2:c.-244_-243insG	NP_000624.2:n.-244_-243insG
NM_000657.2:c.-244_-243insG	NP_000648.2:n.-244_-243insG
XM_011526135.1:c.-244_-243insG	XP_011524437.1:n.-244_-243insG
XR_935246.1:n.869_870insG
XR_935247.1:n.869_870insG
XR_935248.1:n.648_649insG
XM_011526135.3:c.-244_-243insG	XP_011524437.1:n.-244_-243insG
XM_017025917.2:c.-244_-243insG	XP_016881406.1:n.-244_-243insG
XR_935248.3:n.1150_1151insG
NM_000633.3:c.-244_-243insG MANE Select	NP_000624.2:n.-244_-243insG
NM_000657.3:c.-244_-243insG	NP_000648.2:n.-244_-243insG