Canonical Allele Identifier: CA2308718918

Gene: BCL2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318795_63318796delinsAG , CM000680.2:g.63318795_63318796delinsAG	GRCh38
NC_000018.9:g.60986028_60986029delinsAG , CM000680.1:g.60986028_60986029delinsAG	GRCh37
NC_000018.8:g.59137008_59137009delinsAG	NCBI36
NG_009361.1:g.5585_5586delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-130_-129delinsCT MANE Select	ENSP00000329623.3:n.-130_-129delinsCT
ENST00000333681.4:c.-130_-129delinsCT	ENSP00000329623.3:n.-130_-129delinsCT
ENST00000398117.1:c.-130_-129delinsCT	ENSP00000381185.1:n.-130_-129delinsCT
ENST00000589955.2:c.-130_-129delinsCT	ENSP00000466417.1:n.-130_-129delinsCT
NM_000633.2:c.-130_-129delinsCT	NP_000624.2:n.-130_-129delinsCT
NM_000657.2:c.-130_-129delinsCT	NP_000648.2:n.-130_-129delinsCT
XM_011526135.1:c.-130_-129delinsCT	XP_011524437.1:n.-130_-129delinsCT
XR_935246.1:n.983_984delinsCT
XR_935247.1:n.983_984delinsCT
XR_935248.1:n.762_763delinsCT
XM_011526135.3:c.-130_-129delinsCT	XP_011524437.1:n.-130_-129delinsCT
XM_017025917.2:c.-130_-129delinsCT	XP_016881406.1:n.-130_-129delinsCT
XR_935248.3:n.1264_1265delinsCT
NM_000633.3:c.-130_-129delinsCT MANE Select	NP_000624.2:n.-130_-129delinsCT
NM_000657.3:c.-130_-129delinsCT	NP_000648.2:n.-130_-129delinsCT