Canonical Allele Identifier: CA382913819
Gene: CBL HGNC NCBI

Linked Data

COSMIC: COSM41790

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119278537T>C , CM000673.2:g.119278537T>C GRCh38
NC_000011.9:g.119149247T>C , CM000673.1:g.119149247T>C GRCh37
NC_000011.8:g.118654457T>C NCBI36
NG_016808.1:g.77258T>C , LRG_608:g.77258T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000700472.1:c.*707T>C ENSP00000515005.1:n.*707T>C
ENST00000264033.6:c.1255T>C MANE Select ENSP00000264033.3:p.Cys419Arg
ENST00000637974.1:c.1249T>C ENSP00000490763.1:p.Cys417Arg
ENST00000264033.5:c.1255T>C ENSP00000264033.3:p.Cys419Arg
ENST00000634586.1:c.1255T>C ENSP00000489218.1:p.Cys419Arg
ENST00000634840.1:c.1255T>C ENSP00000489324.1:p.Cys419Arg
NM_005188.3:c.1255T>C , LRG_608t1:c.1255T>C NP_005179.2:p.Cys419Arg
XM_011543057.1:c.1255T>C XP_011541359.1:p.Cys419Arg
NM_005188.4:c.1255T>C MANE Select NP_005179.2:p.Cys419Arg