Canonical Allele Identifier: CA2003906322
Gene: CBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119278541G= , CM000673.2:g.119278541G= GRCh38
NC_000011.9:g.119149251G= , CM000673.1:g.119149251G= GRCh37
NC_000011.8:g.118654461G= NCBI36
NG_016808.1:g.77262G= , LRG_608:g.77262G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700472.1:c.*711G= ENSP00000515005.1:n.*711G=
ENST00000264033.6:c.1259G= MANE Select ENSP00000264033.3:p.Arg420=
ENST00000637974.1:c.1253G= ENSP00000490763.1:p.Arg418=
ENST00000264033.5:c.1259G= ENSP00000264033.3:p.Arg420=
ENST00000634586.1:c.1259G= ENSP00000489218.1:p.Arg420=
ENST00000634840.1:c.1259G= ENSP00000489324.1:p.Arg420=
NM_005188.3:c.1259G= , LRG_608t1:c.1259G= NP_005179.2:p.Arg420=
XM_011543057.1:c.1259G= XP_011541359.1:p.Arg420=
NM_005188.4:c.1259G= MANE Select NP_005179.2:p.Arg420=