Canonical Allele Identifier: CA2003905167
Gene: CBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119277776C= , CM000673.2:g.119277776C= GRCh38
NC_000011.9:g.119148486C= , CM000673.1:g.119148486C= GRCh37
NC_000011.8:g.118653696C= NCBI36
NG_016808.1:g.76497C= , LRG_608:g.76497C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700472.1:c.*479C= ENSP00000515005.1:n.*479C=
ENST00000264033.6:c.1027C= MANE Select ENSP00000264033.3:p.Arg343=
ENST00000637974.1:c.1021C= ENSP00000490763.1:p.Arg341=
ENST00000264033.5:c.1027C= ENSP00000264033.3:p.Arg343=
ENST00000634586.1:c.1027C= ENSP00000489218.1:p.Arg343=
ENST00000634840.1:c.1027C= ENSP00000489324.1:p.Arg343=
NM_005188.3:c.1027C= , LRG_608t1:c.1027C= NP_005179.2:p.Arg343=
XM_011543057.1:c.1027C= XP_011541359.1:p.Arg343=
NM_005188.4:c.1027C= MANE Select NP_005179.2:p.Arg343=