Canonical Allele Identifier: CA2003906169

Gene: CBL

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119278375_119278376delinsCA , CM000673.2:g.119278375_119278376delinsCA	GRCh38
NC_000011.9:g.119149085_119149086delinsCA , CM000673.1:g.119149085_119149086delinsCA	GRCh37
NC_000011.8:g.118654295_118654296delinsCA	NCBI36
NG_016808.1:g.77096_77097delinsCA , LRG_608:g.77096_77097delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700472.1:c.*679+78_*679+79delinsCA	ENSP00000515005.1:n.*679+78_*679+79delinsCA
ENST00000264033.6:c.1227+78_1227+79delinsCA MANE Select	ENSP00000264033.3:n.1227+78_1227+79delinsCA
ENST00000637974.1:c.1221+78_1221+79delinsCA	ENSP00000490763.1:n.1221+78_1221+79delinsCA
ENST00000264033.5:c.1227+78_1227+79delinsCA	ENSP00000264033.3:n.1227+78_1227+79delinsCA
ENST00000634586.1:c.1227+78_1227+79delinsCA	ENSP00000489218.1:n.1227+78_1227+79delinsCA
ENST00000634840.1:c.1227+78_1227+79delinsCA	ENSP00000489324.1:n.1227+78_1227+79delinsCA
NM_005188.3:c.1227+78_1227+79delinsCA , LRG_608t1:c.1227+78_1227+79delinsCA	NP_005179.2:n.1227+78_1227+79delinsCA
XM_011543057.1:c.1227+78_1227+79delinsCA	XP_011541359.1:n.1227+78_1227+79delinsCA
NM_005188.4:c.1227+78_1227+79delinsCA MANE Select	NP_005179.2:n.1227+78_1227+79delinsCA