Canonical Allele Identifier: CA2308644520

Gene: BCL2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63153249_63153250delinsTA , CM000680.2:g.63153249_63153250delinsTA	GRCh38
NC_000018.9:g.60820482_60820483delinsTA , CM000680.1:g.60820482_60820483delinsTA	GRCh37
NC_000018.8:g.58971462_58971463delinsTA	NCBI36
NG_009361.1:g.171131_171132delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.586-24491_586-24490delinsTA MANE Select	ENSP00000329623.3:n.586-24491_586-24490delinsTA
ENST00000677227.1:c.914-24491_914-24490delinsTA	ENSP00000504566.1:n.914-24491_914-24490delinsTA
ENST00000678134.1:c.790-24491_790-24490delinsTA	ENSP00000503628.1:n.790-24491_790-24490delinsTA
ENST00000678301.1:c.24+4823_24+4824delinsTA	ENSP00000504546.1:n.24+4823_24+4824delinsTA
ENST00000678349.1:c.1138-24491_1138-24490delinsTA	ENSP00000504190.1:n.1138-24491_1138-24490delinsTA
ENST00000333681.4:c.586-24491_586-24490delinsTA	ENSP00000329623.3:n.586-24491_586-24490delinsTA
ENST00000398117.1:c.586-24491_586-24490delinsTA	ENSP00000381185.1:n.586-24491_586-24490delinsTA
ENST00000590515.1:n.24+8596_24+8597delinsTA
NM_000633.2:c.586-24491_586-24490delinsTA	NP_000624.2:n.586-24491_586-24490delinsTA
XR_935246.1:n.2026-24491_2026-24490delinsTA
XR_935248.1:n.1805-24491_1805-24490delinsTA
XR_935248.3:n.2307-24491_2307-24490delinsTA
NM_000633.3:c.586-24491_586-24490delinsTA MANE Select	NP_000624.2:n.586-24491_586-24490delinsTA