Canonical Allele Identifier: CA657488501

Gene: BCL2

Linked Data

• COSMIC: COSN23393923

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318918_63318919insT , CM000680.2:g.63318918_63318919insT	GRCh38
NC_000018.9:g.60986151_60986152insT , CM000680.1:g.60986151_60986152insT	GRCh37
NC_000018.8:g.59137131_59137132insT	NCBI36
NG_009361.1:g.5462_5463insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-253_-252insA MANE Select	ENSP00000329623.3:n.-253_-252insA
ENST00000333681.4:c.-253_-252insA	ENSP00000329623.3:n.-253_-252insA
ENST00000398117.1:c.-253_-252insA	ENSP00000381185.1:n.-253_-252insA
NM_000633.2:c.-253_-252insA	NP_000624.2:n.-253_-252insA
NM_000657.2:c.-253_-252insA	NP_000648.2:n.-253_-252insA
XM_011526135.1:c.-253_-252insA	XP_011524437.1:n.-253_-252insA
XR_935246.1:n.860_861insA
XR_935247.1:n.860_861insA
XR_935248.1:n.639_640insA
XM_011526135.3:c.-253_-252insA	XP_011524437.1:n.-253_-252insA
XM_017025917.2:c.-253_-252insA	XP_016881406.1:n.-253_-252insA
XR_935248.3:n.1141_1142insA
NM_000633.3:c.-253_-252insA MANE Select	NP_000624.2:n.-253_-252insA
NM_000657.3:c.-253_-252insA	NP_000648.2:n.-253_-252insA