Canonical Allele Identifier: CA2003906129
Gene: CBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119278321T= , CM000673.2:g.119278321T= GRCh38
NC_000011.9:g.119149031T= , CM000673.1:g.119149031T= GRCh37
NC_000011.8:g.118654241T= NCBI36
NG_016808.1:g.77042T= , LRG_608:g.77042T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700472.1:c.*679+24T= ENSP00000515005.1:n.*679+24T=
ENST00000264033.6:c.1227+24T= MANE Select ENSP00000264033.3:n.1227+24T=
ENST00000637974.1:c.1221+24T= ENSP00000490763.1:n.1221+24T=
ENST00000264033.5:c.1227+24T= ENSP00000264033.3:n.1227+24T=
ENST00000634586.1:c.1227+24T= ENSP00000489218.1:n.1227+24T=
ENST00000634840.1:c.1227+24T= ENSP00000489324.1:n.1227+24T=
NM_005188.3:c.1227+24T= , LRG_608t1:c.1227+24T= NP_005179.2:n.1227+24T=
XM_011543057.1:c.1227+24T= XP_011541359.1:n.1227+24T=
NM_005188.4:c.1227+24T= MANE Select NP_005179.2:n.1227+24T=