Canonical Allele Identifier: CA2308718978

Gene: BCL2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318932_63318933delinsCA , CM000680.2:g.63318932_63318933delinsCA	GRCh38
NC_000018.9:g.60986165_60986166delinsCA , CM000680.1:g.60986165_60986166delinsCA	GRCh37
NC_000018.8:g.59137145_59137146delinsCA	NCBI36
NG_009361.1:g.5448_5449delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-267_-266delinsTG MANE Select	ENSP00000329623.3:n.-267_-266delinsTG
ENST00000333681.4:c.-267_-266delinsTG	ENSP00000329623.3:n.-267_-266delinsTG
ENST00000398117.1:c.-267_-266delinsTG	ENSP00000381185.1:n.-267_-266delinsTG
NM_000633.2:c.-267_-266delinsTG	NP_000624.2:n.-267_-266delinsTG
NM_000657.2:c.-267_-266delinsTG	NP_000648.2:n.-267_-266delinsTG
XM_011526135.1:c.-267_-266delinsTG	XP_011524437.1:n.-267_-266delinsTG
XR_935246.1:n.846_847delinsTG
XR_935247.1:n.846_847delinsTG
XR_935248.1:n.625_626delinsTG
XM_011526135.3:c.-267_-266delinsTG	XP_011524437.1:n.-267_-266delinsTG
XM_017025917.2:c.-267_-266delinsTG	XP_016881406.1:n.-267_-266delinsTG
XR_935248.3:n.1127_1128delinsTG
NM_000633.3:c.-267_-266delinsTG MANE Select	NP_000624.2:n.-267_-266delinsTG
NM_000657.3:c.-267_-266delinsTG	NP_000648.2:n.-267_-266delinsTG