Canonical Allele Identifier: CA2003905836
Gene: CBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119278181T= , CM000673.2:g.119278181T= GRCh38
NC_000011.9:g.119148891T= , CM000673.1:g.119148891T= GRCh37
NC_000011.8:g.118654101T= NCBI36
NG_016808.1:g.76902T= , LRG_608:g.76902T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700472.1:c.*563T= ENSP00000515005.1:n.*563T=
ENST00000264033.6:c.1111T= MANE Select ENSP00000264033.3:p.Tyr371=
ENST00000637974.1:c.1105T= ENSP00000490763.1:p.Tyr369=
ENST00000264033.5:c.1111T= ENSP00000264033.3:p.Tyr371=
ENST00000634586.1:c.1111T= ENSP00000489218.1:p.Tyr371=
ENST00000634840.1:c.1111T= ENSP00000489324.1:p.Tyr371=
NM_005188.3:c.1111T= , LRG_608t1:c.1111T= NP_005179.2:p.Tyr371=
XM_011543057.1:c.1111T= XP_011541359.1:p.Tyr371=
NM_005188.4:c.1111T= MANE Select NP_005179.2:p.Tyr371=