Canonical Allele Identifier: CA2308702127
Gene: BCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.63279825_63279826delinsTC , CM000680.2:g.63279825_63279826delinsTC GRCh38
NC_000018.9:g.60947058_60947059delinsTC , CM000680.1:g.60947058_60947059delinsTC GRCh37
NC_000018.8:g.59098038_59098039delinsTC NCBI36
NG_009361.1:g.44555_44556delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000333681.5:c.585+38256_585+38257delinsGA MANE Select ENSP00000329623.3:n.585+38256_585+38257delinsGA
ENST00000677227.1:c.913+1061_913+1062delinsGA ENSP00000504566.1:n.913+1061_913+1062delinsGA
ENST00000678134.1:c.789+21836_789+21837delinsGA ENSP00000503628.1:n.789+21836_789+21837delinsGA
ENST00000678349.1:c.1137+37704_1137+37705delinsGA ENSP00000504190.1:n.1137+37704_1137+37705delinsGA
ENST00000333681.4:c.585+38256_585+38257delinsGA ENSP00000329623.3:n.585+38256_585+38257delinsGA
ENST00000398117.1:c.585+38256_585+38257delinsGA ENSP00000381185.1:n.585+38256_585+38257delinsGA
NM_000633.2:c.585+38256_585+38257delinsGA NP_000624.2:n.585+38256_585+38257delinsGA
XR_935246.1:n.2025+1061_2025+1062delinsGA
XR_935247.1:n.2025+1061_2025+1062delinsGA
XR_935248.1:n.1804+1061_1804+1062delinsGA
XR_935248.3:n.2306+1061_2306+1062delinsGA
NM_000633.3:c.585+38256_585+38257delinsGA MANE Select NP_000624.2:n.585+38256_585+38257delinsGA