Canonical Allele Identifier: CA657488277

Gene: BCL2

Linked Data

• COSMIC: COSN23392503

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318886_63318887insG , CM000680.2:g.63318886_63318887insG	GRCh38
NC_000018.9:g.60986119_60986120insG , CM000680.1:g.60986119_60986120insG	GRCh37
NC_000018.8:g.59137099_59137100insG	NCBI36
NG_009361.1:g.5494_5495insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-221_-220insC MANE Select	ENSP00000329623.3:n.-221_-220insC
ENST00000333681.4:c.-221_-220insC	ENSP00000329623.3:n.-221_-220insC
ENST00000398117.1:c.-221_-220insC	ENSP00000381185.1:n.-221_-220insC
NM_000633.2:c.-221_-220insC	NP_000624.2:n.-221_-220insC
NM_000657.2:c.-221_-220insC	NP_000648.2:n.-221_-220insC
XM_011526135.1:c.-221_-220insC	XP_011524437.1:n.-221_-220insC
XR_935246.1:n.892_893insC
XR_935247.1:n.892_893insC
XR_935248.1:n.671_672insC
XM_011526135.3:c.-221_-220insC	XP_011524437.1:n.-221_-220insC
XM_017025917.2:c.-221_-220insC	XP_016881406.1:n.-221_-220insC
XR_935248.3:n.1173_1174insC
NM_000633.3:c.-221_-220insC MANE Select	NP_000624.2:n.-221_-220insC
NM_000657.3:c.-221_-220insC	NP_000648.2:n.-221_-220insC