Canonical Allele Identifier: CA657488473

Gene: BCL2

Linked Data

• COSMIC: COSN23153153

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318917_63318918insC , CM000680.2:g.63318917_63318918insC	GRCh38
NC_000018.9:g.60986150_60986151insC , CM000680.1:g.60986150_60986151insC	GRCh37
NC_000018.8:g.59137130_59137131insC	NCBI36
NG_009361.1:g.5463_5464insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-252_-251insG MANE Select	ENSP00000329623.3:n.-252_-251insG
ENST00000333681.4:c.-252_-251insG	ENSP00000329623.3:n.-252_-251insG
ENST00000398117.1:c.-252_-251insG	ENSP00000381185.1:n.-252_-251insG
NM_000633.2:c.-252_-251insG	NP_000624.2:n.-252_-251insG
NM_000657.2:c.-252_-251insG	NP_000648.2:n.-252_-251insG
XM_011526135.1:c.-252_-251insG	XP_011524437.1:n.-252_-251insG
XR_935246.1:n.861_862insG
XR_935247.1:n.861_862insG
XR_935248.1:n.640_641insG
XM_011526135.3:c.-252_-251insG	XP_011524437.1:n.-252_-251insG
XM_017025917.2:c.-252_-251insG	XP_016881406.1:n.-252_-251insG
XR_935248.3:n.1142_1143insG
NM_000633.3:c.-252_-251insG MANE Select	NP_000624.2:n.-252_-251insG
NM_000657.3:c.-252_-251insG	NP_000648.2:n.-252_-251insG