Canonical Allele Identifier: CA2551286728

Gene: BCL2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63153381_63153382insTTCTGTAAGCTACTTGTAAATAAAGAAGGTACCTAGGAAAGGAAAATTGCCATCTCTCTCATTTTTGCATT , CM000680.2:g.63153381_63153382insTTCTGTAAGCTACTTGTAAATAAAGAAGGTACCTAGGAAAGGAAAATTGCCATCTCTCTCATTTTTGCATT	GRCh38
NC_000018.9:g.60820614_60820615insTTCTGTAAGCTACTTGTAAATAAAGAAGGTACCTAGGAAAGGAAAATTGCCATCTCTCTCATTTTTGCATT , CM000680.1:g.60820614_60820615insTTCTGTAAGCTACTTGTAAATAAAGAAGGTACCTAGGAAAGGAAAATTGCCATCTCTCTCATTTTTGCATT	GRCh37
NC_000018.8:g.58971594_58971595insTTCTGTAAGCTACTTGTAAATAAAGAAGGTACCTAGGAAAGGAAAATTGCCATCTCTCTCATTTTTGCATT	NCBI36
NG_009361.1:g.171017_171018insATGGCAATTTTCCTTTCCTAGGTACCTTCTTTATTTACAAGTAGCTTACAGAAAATGCAAAAATGAGAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.586-24605_586-24604insATGGCAATTTTCCTTTCCTAGGTACCTTCTTTATTTACAAGTAGCTTACAGAAAATGCAAAAATGAGAGAG MANE Select	ENSP00000329623.3:n.586-24605_586-24604insATGGCAATTTTCCTTTCCT...
ENST00000677227.1:c.914-24605_914-24604insATGGCAATTTTCCTTTCCTAGGTACCTTCTTTATTTACAAGTAGCTTACAGAAAATGCAAAAATGAGAGAG	ENSP00000504566.1:n.914-24605_914-24604insATGGCAATTTTCCTTTCCT...
ENST00000678134.1:c.790-24605_790-24604insATGGCAATTTTCCTTTCCTAGGTACCTTCTTTATTTACAAGTAGCTTACAGAAAATGCAAAAATGAGAGAG	ENSP00000503628.1:n.790-24605_790-24604insATGGCAATTTTCCTTTCCT...
ENST00000678301.1:c.24+4709_24+4710insATGGCAATTTTCCTTTCCTAGGTACCTTCTTTATTTACAAGTAGCTTACAGAAAATGCAAAAATGAGAGAG	ENSP00000504546.1:n.24+4709_24+4710insATGGCAATTTTCCTTTCCTAGGT...
ENST00000678349.1:c.1138-24605_1138-24604insATGGCAATTTTCCTTTCCTAGGTACCTTCTTTATTTACAAGTAGCTTACAGAAAATGCAAAAATGAGAGAG	ENSP00000504190.1:n.1138-24605_1138-24604insATGGCAATTTTCCTTTC...
ENST00000333681.4:c.586-24605_586-24604insATGGCAATTTTCCTTTCCTAGGTACCTTCTTTATTTACAAGTAGCTTACAGAAAATGCAAAAATGAGAGAG	ENSP00000329623.3:n.586-24605_586-24604insATGGCAATTTTCCTTTCCT...
ENST00000398117.1:c.586-24605_586-24604insATGGCAATTTTCCTTTCCTAGGTACCTTCTTTATTTACAAGTAGCTTACAGAAAATGCAAAAATGAGAGAG	ENSP00000381185.1:n.586-24605_586-24604insATGGCAATTTTCCTTTCCT...
ENST00000590515.1:n.24+8482_24+8483insATGGCAATTTTCCTTTCCTAGGTACCTTCTTTATTTACAAGTAGCTTACAGAAAATGCAAAAATGAGAGAG
NM_000633.2:c.586-24605_586-24604insATGGCAATTTTCCTTTCCTAGGTACCTTCTTTATTTACAAGTAGCTTACAGAAAATGCAAAAATGAGAGAG	NP_000624.2:n.586-24605_586-24604insATGGCAATTTTCCTTTCCTAGGTAC...
XR_935246.1:n.2026-24605_2026-24604insATGGCAATTTTCCTTTCCTAGGTACCTTCTTTATTTACAAGTAGCTTACAGAAAATGCAAAAATGAGAGAG
XR_935248.1:n.1805-24605_1805-24604insATGGCAATTTTCCTTTCCTAGGTACCTTCTTTATTTACAAGTAGCTTACAGAAAATGCAAAAATGAGAGAG
XR_935248.3:n.2307-24605_2307-24604insATGGCAATTTTCCTTTCCTAGGTACCTTCTTTATTTACAAGTAGCTTACAGAAAATGCAAAAATGAGAGAG
NM_000633.3:c.586-24605_586-24604insATGGCAATTTTCCTTTCCTAGGTACCTTCTTTATTTACAAGTAGCTTACAGAAAATGCAAAAATGAGAGAG MANE Select	NP_000624.2:n.586-24605_586-24604insATGGCAATTTTCCTTTCCTAGGTAC...