Canonical Allele Identifier: CA2725176357
Gene: CBL HGNC NCBI

Linked Data

dbSNP Id: rs2135304196

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119278398del , CM000673.2:g.119278398del GRCh38
NC_000011.9:g.119149108del , CM000673.1:g.119149108del GRCh37
NC_000011.8:g.118654318del NCBI36
NG_016808.1:g.77119del , LRG_608:g.77119del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700472.1:c.*679+101del ENSP00000515005.1:n.*679+101del
ENST00000264033.6:c.1227+101del MANE Select ENSP00000264033.3:n.1227+101del
ENST00000637974.1:c.1221+101del ENSP00000490763.1:n.1221+101del
ENST00000264033.5:c.1227+101del ENSP00000264033.3:n.1227+101del
ENST00000634586.1:c.1227+101del ENSP00000489218.1:n.1227+101del
ENST00000634840.1:c.1227+101del ENSP00000489324.1:n.1227+101del
NM_005188.3:c.1227+101del , LRG_608t1:c.1227+101del NP_005179.2:n.1227+101del
XM_011543057.1:c.1227+101del XP_011541359.1:n.1227+101del
NM_005188.4:c.1227+101del MANE Select NP_005179.2:n.1227+101del