Canonical Allele Identifier: CA657488064

Gene: BCL2

Linked Data

• COSMIC: COSN23273890

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318769_63318770insG , CM000680.2:g.63318769_63318770insG	GRCh38
NC_000018.9:g.60986002_60986003insG , CM000680.1:g.60986002_60986003insG	GRCh37
NC_000018.8:g.59136982_59136983insG	NCBI36
NG_009361.1:g.5611_5612insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-104_-103insC MANE Select	ENSP00000329623.3:n.-104_-103insC
ENST00000333681.4:c.-104_-103insC	ENSP00000329623.3:n.-104_-103insC
ENST00000398117.1:c.-104_-103insC	ENSP00000381185.1:n.-104_-103insC
ENST00000589955.2:c.-104_-103insC	ENSP00000466417.1:n.-104_-103insC
NM_000633.2:c.-104_-103insC	NP_000624.2:n.-104_-103insC
NM_000657.2:c.-104_-103insC	NP_000648.2:n.-104_-103insC
XM_011526135.1:c.-104_-103insC	XP_011524437.1:n.-104_-103insC
XR_935246.1:n.1009_1010insC
XR_935247.1:n.1009_1010insC
XR_935248.1:n.788_789insC
XM_011526135.3:c.-104_-103insC	XP_011524437.1:n.-104_-103insC
XM_017025917.2:c.-104_-103insC	XP_016881406.1:n.-104_-103insC
XR_935248.3:n.1290_1291insC
NM_000633.3:c.-104_-103insC MANE Select	NP_000624.2:n.-104_-103insC
NM_000657.3:c.-104_-103insC	NP_000648.2:n.-104_-103insC