Canonical Allele Identifier: CA657488239

Gene: BCL2

Linked Data

• COSMIC: COSN25139026

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318873_63318899del , CM000680.2:g.63318873_63318899del	GRCh38
NC_000018.9:g.60986106_60986132del , CM000680.1:g.60986106_60986132del	GRCh37
NC_000018.8:g.59137086_59137112del	NCBI36
NG_009361.1:g.5482_5508del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-233_-207del MANE Select	ENSP00000329623.3:n.-233_-207del
ENST00000333681.4:c.-233_-207del	ENSP00000329623.3:n.-233_-207del
ENST00000398117.1:c.-233_-207del	ENSP00000381185.1:n.-233_-207del
NM_000633.2:c.-233_-207del	NP_000624.2:n.-233_-207del
NM_000657.2:c.-233_-207del	NP_000648.2:n.-233_-207del
XM_011526135.1:c.-233_-207del	XP_011524437.1:n.-233_-207del
XR_935246.1:n.880_906del
XR_935247.1:n.880_906del
XR_935248.1:n.659_685del
XM_011526135.3:c.-233_-207del	XP_011524437.1:n.-233_-207del
XM_017025917.2:c.-233_-207del	XP_016881406.1:n.-233_-207del
XR_935248.3:n.1161_1187del
NM_000633.3:c.-233_-207del MANE Select	NP_000624.2:n.-233_-207del
NM_000657.3:c.-233_-207del	NP_000648.2:n.-233_-207del