Canonical Allele Identifier: CA657487812

Gene: BCL2

Linked Data

• COSMIC: COSN23164628

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318684_63318685insG , CM000680.2:g.63318684_63318685insG	GRCh38
NC_000018.9:g.60985917_60985918insG , CM000680.1:g.60985917_60985918insG	GRCh37
NC_000018.8:g.59136897_59136898insG	NCBI36
NG_009361.1:g.5696_5697insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-19_-18insC MANE Select	ENSP00000329623.3:n.-19_-18insC
ENST00000333681.4:c.-19_-18insC	ENSP00000329623.3:n.-19_-18insC
ENST00000398117.1:c.-19_-18insC	ENSP00000381185.1:n.-19_-18insC
ENST00000589955.2:c.-19_-18insC	ENSP00000466417.1:n.-19_-18insC
NM_000633.2:c.-19_-18insC	NP_000624.2:n.-19_-18insC
NM_000657.2:c.-19_-18insC	NP_000648.2:n.-19_-18insC
XM_011526135.1:c.-19_-18insC	XP_011524437.1:n.-19_-18insC
XR_935246.1:n.1094_1095insC
XR_935247.1:n.1094_1095insC
XR_935248.1:n.873_874insC
XM_011526135.3:c.-19_-18insC	XP_011524437.1:n.-19_-18insC
XM_017025917.2:c.-19_-18insC	XP_016881406.1:n.-19_-18insC
XR_935248.3:n.1375_1376insC
NM_000633.3:c.-19_-18insC MANE Select	NP_000624.2:n.-19_-18insC
NM_000657.3:c.-19_-18insC	NP_000648.2:n.-19_-18insC