Canonical Allele Identifier: CA2003906224

Gene: CBL

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119278459_119278460delinsAT , CM000673.2:g.119278459_119278460delinsAT	GRCh38
NC_000011.9:g.119149169_119149170delinsAT , CM000673.1:g.119149169_119149170delinsAT	GRCh37
NC_000011.8:g.118654379_118654380delinsAT	NCBI36
NG_016808.1:g.77180_77181delinsAT , LRG_608:g.77180_77181delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700472.1:c.*680-51_*680-50delinsAT	ENSP00000515005.1:n.*680-51_*680-50delinsAT
ENST00000264033.6:c.1228-51_1228-50delinsAT MANE Select	ENSP00000264033.3:n.1228-51_1228-50delinsAT
ENST00000637974.1:c.1222-51_1222-50delinsAT	ENSP00000490763.1:n.1222-51_1222-50delinsAT
ENST00000264033.5:c.1228-51_1228-50delinsAT	ENSP00000264033.3:n.1228-51_1228-50delinsAT
ENST00000634586.1:c.1228-51_1228-50delinsAT	ENSP00000489218.1:n.1228-51_1228-50delinsAT
ENST00000634840.1:c.1228-51_1228-50delinsAT	ENSP00000489324.1:n.1228-51_1228-50delinsAT
NM_005188.3:c.1228-51_1228-50delinsAT , LRG_608t1:c.1228-51_1228-50delinsAT	NP_005179.2:n.1228-51_1228-50delinsAT
XM_011543057.1:c.1228-51_1228-50delinsAT	XP_011541359.1:n.1228-51_1228-50delinsAT
NM_005188.4:c.1228-51_1228-50delinsAT MANE Select	NP_005179.2:n.1228-51_1228-50delinsAT