Canonical Allele Identifier: CA657487816

Gene: BCL2

Linked Data

• COSMIC: COSN23380670

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318685_63318686insG , CM000680.2:g.63318685_63318686insG	GRCh38
NC_000018.9:g.60985918_60985919insG , CM000680.1:g.60985918_60985919insG	GRCh37
NC_000018.8:g.59136898_59136899insG	NCBI36
NG_009361.1:g.5695_5696insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-20_-19insC MANE Select	ENSP00000329623.3:n.-20_-19insC
ENST00000333681.4:c.-20_-19insC	ENSP00000329623.3:n.-20_-19insC
ENST00000398117.1:c.-20_-19insC	ENSP00000381185.1:n.-20_-19insC
ENST00000589955.2:c.-20_-19insC	ENSP00000466417.1:n.-20_-19insC
NM_000633.2:c.-20_-19insC	NP_000624.2:n.-20_-19insC
NM_000657.2:c.-20_-19insC	NP_000648.2:n.-20_-19insC
XM_011526135.1:c.-20_-19insC	XP_011524437.1:n.-20_-19insC
XR_935246.1:n.1093_1094insC
XR_935247.1:n.1093_1094insC
XR_935248.1:n.872_873insC
XM_011526135.3:c.-20_-19insC	XP_011524437.1:n.-20_-19insC
XM_017025917.2:c.-20_-19insC	XP_016881406.1:n.-20_-19insC
XR_935248.3:n.1374_1375insC
NM_000633.3:c.-20_-19insC MANE Select	NP_000624.2:n.-20_-19insC
NM_000657.3:c.-20_-19insC	NP_000648.2:n.-20_-19insC