Canonical Allele Identifier: CA2812775404
Gene: BCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.63318921_63318923del , CM000680.2:g.63318921_63318923del GRCh38
NC_000018.9:g.60986154_60986156del , CM000680.1:g.60986154_60986156del GRCh37
NC_000018.8:g.59137134_59137136del NCBI36
NG_009361.1:g.5459_5461del

Transcript Alleles

HGVS Amino-acid Change
ENST00000333681.5:c.-256_-254del MANE Select ENSP00000329623.3:n.-256_-254del
ENST00000333681.4:c.-256_-254del ENSP00000329623.3:n.-256_-254del
ENST00000398117.1:c.-256_-254del ENSP00000381185.1:n.-256_-254del
NM_000633.2:c.-256_-254del NP_000624.2:n.-256_-254del
NM_000657.2:c.-256_-254del NP_000648.2:n.-256_-254del
XM_011526135.1:c.-256_-254del XP_011524437.1:n.-256_-254del
XR_935246.1:n.857_859del
XR_935247.1:n.857_859del
XR_935248.1:n.636_638del
XM_011526135.3:c.-256_-254del XP_011524437.1:n.-256_-254del
XM_017025917.2:c.-256_-254del XP_016881406.1:n.-256_-254del
XR_935248.3:n.1138_1140del
NM_000633.3:c.-256_-254del MANE Select NP_000624.2:n.-256_-254del
NM_000657.3:c.-256_-254del NP_000648.2:n.-256_-254del