Canonical Allele Identifier: CA657488560

Gene: BCL2

Linked Data

• COSMIC: COSN23273892

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318924_63318925insA , CM000680.2:g.63318924_63318925insA	GRCh38
NC_000018.9:g.60986157_60986158insA , CM000680.1:g.60986157_60986158insA	GRCh37
NC_000018.8:g.59137137_59137138insA	NCBI36
NG_009361.1:g.5456_5457insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-259_-258insT MANE Select	ENSP00000329623.3:n.-259_-258insT
ENST00000333681.4:c.-259_-258insT	ENSP00000329623.3:n.-259_-258insT
ENST00000398117.1:c.-259_-258insT	ENSP00000381185.1:n.-259_-258insT
NM_000633.2:c.-259_-258insT	NP_000624.2:n.-259_-258insT
NM_000657.2:c.-259_-258insT	NP_000648.2:n.-259_-258insT
XM_011526135.1:c.-259_-258insT	XP_011524437.1:n.-259_-258insT
XR_935246.1:n.854_855insT
XR_935247.1:n.854_855insT
XR_935248.1:n.633_634insT
XM_011526135.3:c.-259_-258insT	XP_011524437.1:n.-259_-258insT
XM_017025917.2:c.-259_-258insT	XP_016881406.1:n.-259_-258insT
XR_935248.3:n.1135_1136insT
NM_000633.3:c.-259_-258insT MANE Select	NP_000624.2:n.-259_-258insT
NM_000657.3:c.-259_-258insT	NP_000648.2:n.-259_-258insT