Canonical Allele Identifier: CA2003906092
Gene: CBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119278293G= , CM000673.2:g.119278293G= GRCh38
NC_000011.9:g.119149003G= , CM000673.1:g.119149003G= GRCh37
NC_000011.8:g.118654213G= NCBI36
NG_016808.1:g.77014G= , LRG_608:g.77014G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700472.1:c.*675G= ENSP00000515005.1:n.*675G=
ENST00000264033.6:c.1223G= MANE Select ENSP00000264033.3:p.Trp408=
ENST00000637974.1:c.1217G= ENSP00000490763.1:p.Trp406=
ENST00000264033.5:c.1223G= ENSP00000264033.3:p.Trp408=
ENST00000634586.1:c.1223G= ENSP00000489218.1:p.Trp408=
ENST00000634840.1:c.1223G= ENSP00000489324.1:p.Trp408=
NM_005188.3:c.1223G= , LRG_608t1:c.1223G= NP_005179.2:p.Trp408=
XM_011543057.1:c.1223G= XP_011541359.1:p.Trp408=
NM_005188.4:c.1223G= MANE Select NP_005179.2:p.Trp408=