Canonical Allele Identifier: CA657488531

Gene: BCL2

Linked Data

• COSMIC: COSN23300733 ; COSN23379105

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318920_63318921insG , CM000680.2:g.63318920_63318921insG	GRCh38
NC_000018.9:g.60986153_60986154insG , CM000680.1:g.60986153_60986154insG	GRCh37
NC_000018.8:g.59137133_59137134insG	NCBI36
NG_009361.1:g.5460_5461insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-255_-254insC MANE Select	ENSP00000329623.3:n.-255_-254insC
ENST00000333681.4:c.-255_-254insC	ENSP00000329623.3:n.-255_-254insC
ENST00000398117.1:c.-255_-254insC	ENSP00000381185.1:n.-255_-254insC
NM_000633.2:c.-255_-254insC	NP_000624.2:n.-255_-254insC
NM_000657.2:c.-255_-254insC	NP_000648.2:n.-255_-254insC
XM_011526135.1:c.-255_-254insC	XP_011524437.1:n.-255_-254insC
XR_935246.1:n.858_859insC
XR_935247.1:n.858_859insC
XR_935248.1:n.637_638insC
XM_011526135.3:c.-255_-254insC	XP_011524437.1:n.-255_-254insC
XM_017025917.2:c.-255_-254insC	XP_016881406.1:n.-255_-254insC
XR_935248.3:n.1139_1140insC
NM_000633.3:c.-255_-254insC MANE Select	NP_000624.2:n.-255_-254insC
NM_000657.3:c.-255_-254insC	NP_000648.2:n.-255_-254insC