Canonical Allele Identifier: CA657488004

Gene: BCL2

Linked Data

• COSMIC: COSN23294389

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318761dup , CM000680.2:g.63318761dup	GRCh38
NC_000018.9:g.60985994dup , CM000680.1:g.60985994dup	GRCh37
NC_000018.8:g.59136974dup	NCBI36
NG_009361.1:g.5620dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-95dup MANE Select	ENSP00000329623.3:n.-95dup
ENST00000333681.4:c.-95dup	ENSP00000329623.3:n.-95dup
ENST00000398117.1:c.-95dup	ENSP00000381185.1:n.-95dup
ENST00000589955.2:c.-95dup	ENSP00000466417.1:n.-95dup
NM_000633.2:c.-95dup	NP_000624.2:n.-95dup
NM_000657.2:c.-95dup	NP_000648.2:n.-95dup
XM_011526135.1:c.-95dup	XP_011524437.1:n.-95dup
XR_935246.1:n.1018dup
XR_935247.1:n.1018dup
XR_935248.1:n.797dup
XM_011526135.3:c.-95dup	XP_011524437.1:n.-95dup
XM_017025917.2:c.-95dup	XP_016881406.1:n.-95dup
XR_935248.3:n.1299dup
NM_000633.3:c.-95dup MANE Select	NP_000624.2:n.-95dup
NM_000657.3:c.-95dup	NP_000648.2:n.-95dup