Canonical Allele Identifier: CA657488398

Gene: BCL2

Linked Data

• COSMIC: COSN23120769

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318908_63318909insC , CM000680.2:g.63318908_63318909insC	GRCh38
NC_000018.9:g.60986141_60986142insC , CM000680.1:g.60986141_60986142insC	GRCh37
NC_000018.8:g.59137121_59137122insC	NCBI36
NG_009361.1:g.5472_5473insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-243_-242insG MANE Select	ENSP00000329623.3:n.-243_-242insG
ENST00000333681.4:c.-243_-242insG	ENSP00000329623.3:n.-243_-242insG
ENST00000398117.1:c.-243_-242insG	ENSP00000381185.1:n.-243_-242insG
NM_000633.2:c.-243_-242insG	NP_000624.2:n.-243_-242insG
NM_000657.2:c.-243_-242insG	NP_000648.2:n.-243_-242insG
XM_011526135.1:c.-243_-242insG	XP_011524437.1:n.-243_-242insG
XR_935246.1:n.870_871insG
XR_935247.1:n.870_871insG
XR_935248.1:n.649_650insG
XM_011526135.3:c.-243_-242insG	XP_011524437.1:n.-243_-242insG
XM_017025917.2:c.-243_-242insG	XP_016881406.1:n.-243_-242insG
XR_935248.3:n.1151_1152insG
NM_000633.3:c.-243_-242insG MANE Select	NP_000624.2:n.-243_-242insG
NM_000657.3:c.-243_-242insG	NP_000648.2:n.-243_-242insG