Canonical Allele Identifier: CA2003905942
Gene: CBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119278217A= , CM000673.2:g.119278217A= GRCh38
NC_000011.9:g.119148927A= , CM000673.1:g.119148927A= GRCh37
NC_000011.8:g.118654137A= NCBI36
NG_016808.1:g.76938A= , LRG_608:g.76938A=

Transcript Alleles

HGVS Amino-acid change
ENST00000700472.1:c.*599A= ENSP00000515005.1:n.*599A=
ENST00000264033.6:c.1147A= MANE Select ENSP00000264033.3:p.Ile383=
ENST00000637974.1:c.1141A= ENSP00000490763.1:p.Ile381=
ENST00000264033.5:c.1147A= ENSP00000264033.3:p.Ile383=
ENST00000634586.1:c.1147A= ENSP00000489218.1:p.Ile383=
ENST00000634840.1:c.1147A= ENSP00000489324.1:p.Ile383=
NM_005188.3:c.1147A= , LRG_608t1:c.1147A= NP_005179.2:p.Ile383=
XM_011543057.1:c.1147A= XP_011541359.1:p.Ile383=
NM_005188.4:c.1147A= MANE Select NP_005179.2:p.Ile383=