Canonical Allele Identifier: CA2308702128
Gene: BCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.63279830_63279835delinsATGAAG , CM000680.2:g.63279830_63279835delinsATGAAG GRCh38
NC_000018.9:g.60947063_60947068delinsATGAAG , CM000680.1:g.60947063_60947068delinsATGAAG GRCh37
NC_000018.8:g.59098043_59098048delinsATGAAG NCBI36
NG_009361.1:g.44546_44551delinsCTTCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000333681.5:c.585+38247_585+38252delinsCTTCAT MANE Select ENSP00000329623.3:n.585+38247_585+38252delinsCTTCAT
ENST00000677227.1:c.913+1052_913+1057delinsCTTCAT ENSP00000504566.1:n.913+1052_913+1057delinsCTTCAT
ENST00000678134.1:c.789+21827_789+21832delinsCTTCAT ENSP00000503628.1:n.789+21827_789+21832delinsCTTCAT
ENST00000678349.1:c.1137+37695_1137+37700delinsCTTCAT ENSP00000504190.1:n.1137+37695_1137+37700delinsCTTCAT
ENST00000333681.4:c.585+38247_585+38252delinsCTTCAT ENSP00000329623.3:n.585+38247_585+38252delinsCTTCAT
ENST00000398117.1:c.585+38247_585+38252delinsCTTCAT ENSP00000381185.1:n.585+38247_585+38252delinsCTTCAT
NM_000633.2:c.585+38247_585+38252delinsCTTCAT NP_000624.2:n.585+38247_585+38252delinsCTTCAT
XR_935246.1:n.2025+1052_2025+1057delinsCTTCAT
XR_935247.1:n.2025+1052_2025+1057delinsCTTCAT
XR_935248.1:n.1804+1052_1804+1057delinsCTTCAT
XR_935248.3:n.2306+1052_2306+1057delinsCTTCAT
NM_000633.3:c.585+38247_585+38252delinsCTTCAT MANE Select NP_000624.2:n.585+38247_585+38252delinsCTTCAT