Canonical Allele Identifier: CA657488626

Gene: BCL2

Linked Data

• COSMIC: COSN23282066

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318934_63318935insA , CM000680.2:g.63318934_63318935insA	GRCh38
NC_000018.9:g.60986167_60986168insA , CM000680.1:g.60986167_60986168insA	GRCh37
NC_000018.8:g.59137147_59137148insA	NCBI36
NG_009361.1:g.5446_5447insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-269_-268insT MANE Select	ENSP00000329623.3:n.-269_-268insT
ENST00000333681.4:c.-269_-268insT	ENSP00000329623.3:n.-269_-268insT
ENST00000398117.1:c.-269_-268insT	ENSP00000381185.1:n.-269_-268insT
NM_000633.2:c.-269_-268insT	NP_000624.2:n.-269_-268insT
NM_000657.2:c.-269_-268insT	NP_000648.2:n.-269_-268insT
XM_011526135.1:c.-269_-268insT	XP_011524437.1:n.-269_-268insT
XR_935246.1:n.844_845insT
XR_935247.1:n.844_845insT
XR_935248.1:n.623_624insT
XM_011526135.3:c.-269_-268insT	XP_011524437.1:n.-269_-268insT
XM_017025917.2:c.-269_-268insT	XP_016881406.1:n.-269_-268insT
XR_935248.3:n.1125_1126insT
NM_000633.3:c.-269_-268insT MANE Select	NP_000624.2:n.-269_-268insT
NM_000657.3:c.-269_-268insT	NP_000648.2:n.-269_-268insT