Canonical Allele Identifier: CA657488378

Gene: BCL2

Linked Data

• COSMIC: COSN23385734

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318905dup , CM000680.2:g.63318905dup	GRCh38
NC_000018.9:g.60986138dup , CM000680.1:g.60986138dup	GRCh37
NC_000018.8:g.59137118dup	NCBI36
NG_009361.1:g.5476dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-239dup MANE Select	ENSP00000329623.3:n.-239dup
ENST00000333681.4:c.-239dup	ENSP00000329623.3:n.-239dup
ENST00000398117.1:c.-239dup	ENSP00000381185.1:n.-239dup
NM_000633.2:c.-239dup	NP_000624.2:n.-239dup
NM_000657.2:c.-239dup	NP_000648.2:n.-239dup
XM_011526135.1:c.-239dup	XP_011524437.1:n.-239dup
XR_935246.1:n.874dup
XR_935247.1:n.874dup
XR_935248.1:n.653dup
XM_011526135.3:c.-239dup	XP_011524437.1:n.-239dup
XM_017025917.2:c.-239dup	XP_016881406.1:n.-239dup
XR_935248.3:n.1155dup
NM_000633.3:c.-239dup MANE Select	NP_000624.2:n.-239dup
NM_000657.3:c.-239dup	NP_000648.2:n.-239dup