Canonical Allele Identifier: CA657488635

Gene: BCL2

Linked Data

• COSMIC: COSN23379106

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318938_63318939insT , CM000680.2:g.63318938_63318939insT	GRCh38
NC_000018.9:g.60986171_60986172insT , CM000680.1:g.60986171_60986172insT	GRCh37
NC_000018.8:g.59137151_59137152insT	NCBI36
NG_009361.1:g.5442_5443insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-273_-272insA MANE Select	ENSP00000329623.3:n.-273_-272insA
ENST00000333681.4:c.-273_-272insA	ENSP00000329623.3:n.-273_-272insA
ENST00000398117.1:c.-273_-272insA	ENSP00000381185.1:n.-273_-272insA
NM_000633.2:c.-273_-272insA	NP_000624.2:n.-273_-272insA
NM_000657.2:c.-273_-272insA	NP_000648.2:n.-273_-272insA
XM_011526135.1:c.-273_-272insA	XP_011524437.1:n.-273_-272insA
XR_935246.1:n.840_841insA
XR_935247.1:n.840_841insA
XR_935248.1:n.619_620insA
XM_011526135.3:c.-273_-272insA	XP_011524437.1:n.-273_-272insA
XM_017025917.2:c.-273_-272insA	XP_016881406.1:n.-273_-272insA
XR_935248.3:n.1121_1122insA
NM_000633.3:c.-273_-272insA MANE Select	NP_000624.2:n.-273_-272insA
NM_000657.3:c.-273_-272insA	NP_000648.2:n.-273_-272insA