Canonical Allele Identifier: CA657488141

Gene: BCL2

Linked Data

• COSMIC: COSN23235024

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318820_63318821insT , CM000680.2:g.63318820_63318821insT	GRCh38
NC_000018.9:g.60986053_60986054insT , CM000680.1:g.60986053_60986054insT	GRCh37
NC_000018.8:g.59137033_59137034insT	NCBI36
NG_009361.1:g.5560_5561insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-155_-154insA MANE Select	ENSP00000329623.3:n.-155_-154insA
ENST00000333681.4:c.-155_-154insA	ENSP00000329623.3:n.-155_-154insA
ENST00000398117.1:c.-155_-154insA	ENSP00000381185.1:n.-155_-154insA
NM_000633.2:c.-155_-154insA	NP_000624.2:n.-155_-154insA
NM_000657.2:c.-155_-154insA	NP_000648.2:n.-155_-154insA
XM_011526135.1:c.-155_-154insA	XP_011524437.1:n.-155_-154insA
XR_935246.1:n.958_959insA
XR_935247.1:n.958_959insA
XR_935248.1:n.737_738insA
XM_011526135.3:c.-155_-154insA	XP_011524437.1:n.-155_-154insA
XM_017025917.2:c.-155_-154insA	XP_016881406.1:n.-155_-154insA
XR_935248.3:n.1239_1240insA
NM_000633.3:c.-155_-154insA MANE Select	NP_000624.2:n.-155_-154insA
NM_000657.3:c.-155_-154insA	NP_000648.2:n.-155_-154insA