Canonical Allele Identifier: CA2308718957

Gene: BCL2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318879_63318885delinsTTTCGGA , CM000680.2:g.63318879_63318885delinsTTTCGGA	GRCh38
NC_000018.9:g.60986112_60986118delinsTTTCGGA , CM000680.1:g.60986112_60986118delinsTTTCGGA	GRCh37
NC_000018.8:g.59137092_59137098delinsTTTCGGA	NCBI36
NG_009361.1:g.5496_5502delinsTCCGAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-219_-213delinsTCCGAAA MANE Select	ENSP00000329623.3:n.-219_-213delinsTCCGAAA
ENST00000333681.4:c.-219_-213delinsTCCGAAA	ENSP00000329623.3:n.-219_-213delinsTCCGAAA
ENST00000398117.1:c.-219_-213delinsTCCGAAA	ENSP00000381185.1:n.-219_-213delinsTCCGAAA
NM_000633.2:c.-219_-213delinsTCCGAAA	NP_000624.2:n.-219_-213delinsTCCGAAA
NM_000657.2:c.-219_-213delinsTCCGAAA	NP_000648.2:n.-219_-213delinsTCCGAAA
XM_011526135.1:c.-219_-213delinsTCCGAAA	XP_011524437.1:n.-219_-213delinsTCCGAAA
XR_935246.1:n.894_900delinsTCCGAAA
XR_935247.1:n.894_900delinsTCCGAAA
XR_935248.1:n.673_679delinsTCCGAAA
XM_011526135.3:c.-219_-213delinsTCCGAAA	XP_011524437.1:n.-219_-213delinsTCCGAAA
XM_017025917.2:c.-219_-213delinsTCCGAAA	XP_016881406.1:n.-219_-213delinsTCCGAAA
XR_935248.3:n.1175_1181delinsTCCGAAA
NM_000633.3:c.-219_-213delinsTCCGAAA MANE Select	NP_000624.2:n.-219_-213delinsTCCGAAA
NM_000657.3:c.-219_-213delinsTCCGAAA	NP_000648.2:n.-219_-213delinsTCCGAAA