Canonical Allele Identifier: CA657488479

Gene: BCL2

Linked Data

• COSMIC: COSN23297453

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318917_63318918insG , CM000680.2:g.63318917_63318918insG	GRCh38
NC_000018.9:g.60986150_60986151insG , CM000680.1:g.60986150_60986151insG	GRCh37
NC_000018.8:g.59137130_59137131insG	NCBI36
NG_009361.1:g.5463_5464insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-252_-251insC MANE Select	ENSP00000329623.3:n.-252_-251insC
ENST00000333681.4:c.-252_-251insC	ENSP00000329623.3:n.-252_-251insC
ENST00000398117.1:c.-252_-251insC	ENSP00000381185.1:n.-252_-251insC
NM_000633.2:c.-252_-251insC	NP_000624.2:n.-252_-251insC
NM_000657.2:c.-252_-251insC	NP_000648.2:n.-252_-251insC
XM_011526135.1:c.-252_-251insC	XP_011524437.1:n.-252_-251insC
XR_935246.1:n.861_862insC
XR_935247.1:n.861_862insC
XR_935248.1:n.640_641insC
XM_011526135.3:c.-252_-251insC	XP_011524437.1:n.-252_-251insC
XM_017025917.2:c.-252_-251insC	XP_016881406.1:n.-252_-251insC
XR_935248.3:n.1142_1143insC
NM_000633.3:c.-252_-251insC MANE Select	NP_000624.2:n.-252_-251insC
NM_000657.3:c.-252_-251insC	NP_000648.2:n.-252_-251insC