Canonical Allele Identifier: CA657488198

Gene: BCL2

Linked Data

• COSMIC: COSN23341811

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318850dup , CM000680.2:g.63318850dup	GRCh38
NC_000018.9:g.60986083dup , CM000680.1:g.60986083dup	GRCh37
NC_000018.8:g.59137063dup	NCBI36
NG_009361.1:g.5531dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-184dup MANE Select	ENSP00000329623.3:n.-184dup
ENST00000333681.4:c.-184dup	ENSP00000329623.3:n.-184dup
ENST00000398117.1:c.-184dup	ENSP00000381185.1:n.-184dup
NM_000633.2:c.-184dup	NP_000624.2:n.-184dup
NM_000657.2:c.-184dup	NP_000648.2:n.-184dup
XM_011526135.1:c.-184dup	XP_011524437.1:n.-184dup
XR_935246.1:n.929dup
XR_935247.1:n.929dup
XR_935248.1:n.708dup
XM_011526135.3:c.-184dup	XP_011524437.1:n.-184dup
XM_017025917.2:c.-184dup	XP_016881406.1:n.-184dup
XR_935248.3:n.1210dup
NM_000633.3:c.-184dup MANE Select	NP_000624.2:n.-184dup
NM_000657.3:c.-184dup	NP_000648.2:n.-184dup