Canonical Allele Identifier: CA2003862813
Gene: CBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119206444_119206445delinsTG , CM000673.2:g.119206444_119206445delinsTG GRCh38
NC_000011.9:g.119077154_119077155delinsTG , CM000673.1:g.119077154_119077155delinsTG GRCh37
NC_000011.8:g.118582364_118582365delinsTG NCBI36
NG_016808.1:g.5165_5166delinsTG , LRG_608:g.5165_5166delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700472.1:c.27_28delinsTG ENSP00000515005.1:p.Ser9=
ENST00000264033.6:c.27_28delinsTG MANE Select ENSP00000264033.3:p.Ser9=
ENST00000637974.1:c.21_22delinsTG ENSP00000490763.1:p.Ser7=
ENST00000264033.5:c.27_28delinsTG ENSP00000264033.3:p.Ser9=
ENST00000634586.1:c.27_28delinsTG ENSP00000489218.1:p.Ser9=
ENST00000634840.1:c.27_28delinsTG ENSP00000489324.1:p.Ser9=
NM_005188.3:c.27_28delinsTG , LRG_608t1:c.27_28delinsTG NP_005179.2:p.Ser9=
XM_011543057.1:c.27_28delinsTG XP_011541359.1:p.Ser9=
NM_005188.4:c.27_28delinsTG MANE Select NP_005179.2:p.Ser9=