Canonical Allele Identifier: CA2003906199

Gene: CBL

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119278416_119278417delinsCT , CM000673.2:g.119278416_119278417delinsCT	GRCh38
NC_000011.9:g.119149126_119149127delinsCT , CM000673.1:g.119149126_119149127delinsCT	GRCh37
NC_000011.8:g.118654336_118654337delinsCT	NCBI36
NG_016808.1:g.77137_77138delinsCT , LRG_608:g.77137_77138delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700472.1:c.*680-94_*680-93delinsCT	ENSP00000515005.1:n.*680-94_*680-93delinsCT
ENST00000264033.6:c.1228-94_1228-93delinsCT MANE Select	ENSP00000264033.3:n.1228-94_1228-93delinsCT
ENST00000637974.1:c.1222-94_1222-93delinsCT	ENSP00000490763.1:n.1222-94_1222-93delinsCT
ENST00000264033.5:c.1228-94_1228-93delinsCT	ENSP00000264033.3:n.1228-94_1228-93delinsCT
ENST00000634586.1:c.1228-94_1228-93delinsCT	ENSP00000489218.1:n.1228-94_1228-93delinsCT
ENST00000634840.1:c.1228-94_1228-93delinsCT	ENSP00000489324.1:n.1228-94_1228-93delinsCT
NM_005188.3:c.1228-94_1228-93delinsCT , LRG_608t1:c.1228-94_1228-93delinsCT	NP_005179.2:n.1228-94_1228-93delinsCT
XM_011543057.1:c.1228-94_1228-93delinsCT	XP_011541359.1:n.1228-94_1228-93delinsCT
NM_005188.4:c.1228-94_1228-93delinsCT MANE Select	NP_005179.2:n.1228-94_1228-93delinsCT