Canonical Allele Identifier: CA657488099

Gene: BCL2

Linked Data

• COSMIC: COSN23391228

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318781_63318782insC , CM000680.2:g.63318781_63318782insC	GRCh38
NC_000018.9:g.60986014_60986015insC , CM000680.1:g.60986014_60986015insC	GRCh37
NC_000018.8:g.59136994_59136995insC	NCBI36
NG_009361.1:g.5599_5600insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-116_-115insG MANE Select	ENSP00000329623.3:n.-116_-115insG
ENST00000333681.4:c.-116_-115insG	ENSP00000329623.3:n.-116_-115insG
ENST00000398117.1:c.-116_-115insG	ENSP00000381185.1:n.-116_-115insG
ENST00000589955.2:c.-116_-115insG	ENSP00000466417.1:n.-116_-115insG
NM_000633.2:c.-116_-115insG	NP_000624.2:n.-116_-115insG
NM_000657.2:c.-116_-115insG	NP_000648.2:n.-116_-115insG
XM_011526135.1:c.-116_-115insG	XP_011524437.1:n.-116_-115insG
XR_935246.1:n.997_998insG
XR_935247.1:n.997_998insG
XR_935248.1:n.776_777insG
XM_011526135.3:c.-116_-115insG	XP_011524437.1:n.-116_-115insG
XM_017025917.2:c.-116_-115insG	XP_016881406.1:n.-116_-115insG
XR_935248.3:n.1278_1279insG
NM_000633.3:c.-116_-115insG MANE Select	NP_000624.2:n.-116_-115insG
NM_000657.3:c.-116_-115insG	NP_000648.2:n.-116_-115insG