Canonical Allele Identifier: CA991099253
Gene: BCL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.63153348_63153349del , CM000680.2:g.63153348_63153349del GRCh38
NC_000018.9:g.60820581_60820582del , CM000680.1:g.60820581_60820582del GRCh37
NC_000018.8:g.58971561_58971562del NCBI36
NG_009361.1:g.171032_171033del

Transcript Alleles

HGVS Amino-acid Change
ENST00000333681.5:c.586-24590_586-24589del MANE Select ENSP00000329623.3:n.586-24590_586-24589del
ENST00000677227.1:c.914-24590_914-24589del ENSP00000504566.1:n.914-24590_914-24589del
ENST00000678134.1:c.790-24590_790-24589del ENSP00000503628.1:n.790-24590_790-24589del
ENST00000678301.1:c.24+4724_24+4725del ENSP00000504546.1:n.24+4724_24+4725del
ENST00000678349.1:c.1138-24590_1138-24589del ENSP00000504190.1:n.1138-24590_1138-24589del
ENST00000333681.4:c.586-24590_586-24589del ENSP00000329623.3:n.586-24590_586-24589del
ENST00000398117.1:c.586-24590_586-24589del ENSP00000381185.1:n.586-24590_586-24589del
ENST00000590515.1:n.24+8497_24+8498del
NM_000633.2:c.586-24590_586-24589del NP_000624.2:n.586-24590_586-24589del
XR_935246.1:n.2026-24590_2026-24589del
XR_935248.1:n.1805-24590_1805-24589del
XR_935248.3:n.2307-24590_2307-24589del
NM_000633.3:c.586-24590_586-24589del MANE Select NP_000624.2:n.586-24590_586-24589del