Canonical Allele Identifier: CA657488337

Gene: BCL2

Linked Data

• COSMIC: COSN23116090

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318902dup , CM000680.2:g.63318902dup	GRCh38
NC_000018.9:g.60986135dup , CM000680.1:g.60986135dup	GRCh37
NC_000018.8:g.59137115dup	NCBI36
NG_009361.1:g.5479dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-236dup MANE Select	ENSP00000329623.3:n.-236dup
ENST00000333681.4:c.-236dup	ENSP00000329623.3:n.-236dup
ENST00000398117.1:c.-236dup	ENSP00000381185.1:n.-236dup
NM_000633.2:c.-236dup	NP_000624.2:n.-236dup
NM_000657.2:c.-236dup	NP_000648.2:n.-236dup
XM_011526135.1:c.-236dup	XP_011524437.1:n.-236dup
XR_935246.1:n.877dup
XR_935247.1:n.877dup
XR_935248.1:n.656dup
XM_011526135.3:c.-236dup	XP_011524437.1:n.-236dup
XM_017025917.2:c.-236dup	XP_016881406.1:n.-236dup
XR_935248.3:n.1158dup
NM_000633.3:c.-236dup MANE Select	NP_000624.2:n.-236dup
NM_000657.3:c.-236dup	NP_000648.2:n.-236dup