Canonical Allele Identifier: CA657488109

Gene: BCL2

Linked Data

• COSMIC: COSN23301335

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318783_63318784insT , CM000680.2:g.63318783_63318784insT	GRCh38
NC_000018.9:g.60986016_60986017insT , CM000680.1:g.60986016_60986017insT	GRCh37
NC_000018.8:g.59136996_59136997insT	NCBI36
NG_009361.1:g.5597_5598insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-118_-117insA MANE Select	ENSP00000329623.3:n.-118_-117insA
ENST00000333681.4:c.-118_-117insA	ENSP00000329623.3:n.-118_-117insA
ENST00000398117.1:c.-118_-117insA	ENSP00000381185.1:n.-118_-117insA
ENST00000589955.2:c.-118_-117insA	ENSP00000466417.1:n.-118_-117insA
NM_000633.2:c.-118_-117insA	NP_000624.2:n.-118_-117insA
NM_000657.2:c.-118_-117insA	NP_000648.2:n.-118_-117insA
XM_011526135.1:c.-118_-117insA	XP_011524437.1:n.-118_-117insA
XR_935246.1:n.995_996insA
XR_935247.1:n.995_996insA
XR_935248.1:n.774_775insA
XM_011526135.3:c.-118_-117insA	XP_011524437.1:n.-118_-117insA
XM_017025917.2:c.-118_-117insA	XP_016881406.1:n.-118_-117insA
XR_935248.3:n.1276_1277insA
NM_000633.3:c.-118_-117insA MANE Select	NP_000624.2:n.-118_-117insA
NM_000657.3:c.-118_-117insA	NP_000648.2:n.-118_-117insA