Canonical Allele Identifier: CA2003906193
Gene: CBL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119278404T= , CM000673.2:g.119278404T= GRCh38
NC_000011.9:g.119149114T= , CM000673.1:g.119149114T= GRCh37
NC_000011.8:g.118654324T= NCBI36
NG_016808.1:g.77125T= , LRG_608:g.77125T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700472.1:c.*680-106T= ENSP00000515005.1:n.*680-106T=
ENST00000264033.6:c.1228-106T= MANE Select ENSP00000264033.3:n.1228-106T=
ENST00000637974.1:c.1222-106T= ENSP00000490763.1:n.1222-106T=
ENST00000264033.5:c.1228-106T= ENSP00000264033.3:n.1228-106T=
ENST00000634586.1:c.1228-106T= ENSP00000489218.1:n.1228-106T=
ENST00000634840.1:c.1228-106T= ENSP00000489324.1:n.1228-106T=
NM_005188.3:c.1228-106T= , LRG_608t1:c.1228-106T= NP_005179.2:n.1228-106T=
XM_011543057.1:c.1228-106T= XP_011541359.1:n.1228-106T=
NM_005188.4:c.1228-106T= MANE Select NP_005179.2:n.1228-106T=
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