Canonical Allele Identifier: CA657488439

Gene: BCL2

Linked Data

• COSMIC: COSN23236836

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318913_63318914insG , CM000680.2:g.63318913_63318914insG	GRCh38
NC_000018.9:g.60986146_60986147insG , CM000680.1:g.60986146_60986147insG	GRCh37
NC_000018.8:g.59137126_59137127insG	NCBI36
NG_009361.1:g.5467_5468insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-248_-247insC MANE Select	ENSP00000329623.3:n.-248_-247insC
ENST00000333681.4:c.-248_-247insC	ENSP00000329623.3:n.-248_-247insC
ENST00000398117.1:c.-248_-247insC	ENSP00000381185.1:n.-248_-247insC
NM_000633.2:c.-248_-247insC	NP_000624.2:n.-248_-247insC
NM_000657.2:c.-248_-247insC	NP_000648.2:n.-248_-247insC
XM_011526135.1:c.-248_-247insC	XP_011524437.1:n.-248_-247insC
XR_935246.1:n.865_866insC
XR_935247.1:n.865_866insC
XR_935248.1:n.644_645insC
XM_011526135.3:c.-248_-247insC	XP_011524437.1:n.-248_-247insC
XM_017025917.2:c.-248_-247insC	XP_016881406.1:n.-248_-247insC
XR_935248.3:n.1146_1147insC
NM_000633.3:c.-248_-247insC MANE Select	NP_000624.2:n.-248_-247insC
NM_000657.3:c.-248_-247insC	NP_000648.2:n.-248_-247insC