Canonical Allele Identifier: CA657488093

Gene: BCL2

Linked Data

• COSMIC: COSN23382328

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318777_63318778insA , CM000680.2:g.63318777_63318778insA	GRCh38
NC_000018.9:g.60986010_60986011insA , CM000680.1:g.60986010_60986011insA	GRCh37
NC_000018.8:g.59136990_59136991insA	NCBI36
NG_009361.1:g.5603_5604insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-112_-111insT MANE Select	ENSP00000329623.3:n.-112_-111insT
ENST00000333681.4:c.-112_-111insT	ENSP00000329623.3:n.-112_-111insT
ENST00000398117.1:c.-112_-111insT	ENSP00000381185.1:n.-112_-111insT
ENST00000589955.2:c.-112_-111insT	ENSP00000466417.1:n.-112_-111insT
NM_000633.2:c.-112_-111insT	NP_000624.2:n.-112_-111insT
NM_000657.2:c.-112_-111insT	NP_000648.2:n.-112_-111insT
XM_011526135.1:c.-112_-111insT	XP_011524437.1:n.-112_-111insT
XR_935246.1:n.1001_1002insT
XR_935247.1:n.1001_1002insT
XR_935248.1:n.780_781insT
XM_011526135.3:c.-112_-111insT	XP_011524437.1:n.-112_-111insT
XM_017025917.2:c.-112_-111insT	XP_016881406.1:n.-112_-111insT
XR_935248.3:n.1282_1283insT
NM_000633.3:c.-112_-111insT MANE Select	NP_000624.2:n.-112_-111insT
NM_000657.3:c.-112_-111insT	NP_000648.2:n.-112_-111insT