Canonical Allele Identifier: CA657488137

Gene: BCL2

Linked Data

• COSMIC: COSN23054129

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318814dup , CM000680.2:g.63318814dup	GRCh38
NC_000018.9:g.60986047dup , CM000680.1:g.60986047dup	GRCh37
NC_000018.8:g.59137027dup	NCBI36
NG_009361.1:g.5567dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-148dup MANE Select	ENSP00000329623.3:n.-148dup
ENST00000333681.4:c.-148dup	ENSP00000329623.3:n.-148dup
ENST00000398117.1:c.-148dup	ENSP00000381185.1:n.-148dup
NM_000633.2:c.-148dup	NP_000624.2:n.-148dup
NM_000657.2:c.-148dup	NP_000648.2:n.-148dup
XM_011526135.1:c.-148dup	XP_011524437.1:n.-148dup
XR_935246.1:n.965dup
XR_935247.1:n.965dup
XR_935248.1:n.744dup
XM_011526135.3:c.-148dup	XP_011524437.1:n.-148dup
XM_017025917.2:c.-148dup	XP_016881406.1:n.-148dup
XR_935248.3:n.1246dup
NM_000633.3:c.-148dup MANE Select	NP_000624.2:n.-148dup
NM_000657.3:c.-148dup	NP_000648.2:n.-148dup