Canonical Allele Identifier: CA657488466

Gene: BCL2

Linked Data

• COSMIC: COSN23234313

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318915_63318916insA , CM000680.2:g.63318915_63318916insA	GRCh38
NC_000018.9:g.60986148_60986149insA , CM000680.1:g.60986148_60986149insA	GRCh37
NC_000018.8:g.59137128_59137129insA	NCBI36
NG_009361.1:g.5465_5466insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-250_-249insT MANE Select	ENSP00000329623.3:n.-250_-249insT
ENST00000333681.4:c.-250_-249insT	ENSP00000329623.3:n.-250_-249insT
ENST00000398117.1:c.-250_-249insT	ENSP00000381185.1:n.-250_-249insT
NM_000633.2:c.-250_-249insT	NP_000624.2:n.-250_-249insT
NM_000657.2:c.-250_-249insT	NP_000648.2:n.-250_-249insT
XM_011526135.1:c.-250_-249insT	XP_011524437.1:n.-250_-249insT
XR_935246.1:n.863_864insT
XR_935247.1:n.863_864insT
XR_935248.1:n.642_643insT
XM_011526135.3:c.-250_-249insT	XP_011524437.1:n.-250_-249insT
XM_017025917.2:c.-250_-249insT	XP_016881406.1:n.-250_-249insT
XR_935248.3:n.1144_1145insT
NM_000633.3:c.-250_-249insT MANE Select	NP_000624.2:n.-250_-249insT
NM_000657.3:c.-250_-249insT	NP_000648.2:n.-250_-249insT