Canonical Allele Identifier: CA2725176371

Gene: CBL

Linked Data

• dbSNP Id: rs2135304254

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119278447_119278473del , CM000673.2:g.119278447_119278473del	GRCh38
NC_000011.9:g.119149157_119149183del , CM000673.1:g.119149157_119149183del	GRCh37
NC_000011.8:g.118654367_118654393del	NCBI36
NG_016808.1:g.77168_77194del , LRG_608:g.77168_77194del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700472.1:c.*680-63_*680-37del	ENSP00000515005.1:n.*680-63_*680-37del
ENST00000264033.6:c.1228-63_1228-37del MANE Select	ENSP00000264033.3:n.1228-63_1228-37del
ENST00000637974.1:c.1222-63_1222-37del	ENSP00000490763.1:n.1222-63_1222-37del
ENST00000264033.5:c.1228-63_1228-37del	ENSP00000264033.3:n.1228-63_1228-37del
ENST00000634586.1:c.1228-63_1228-37del	ENSP00000489218.1:n.1228-63_1228-37del
ENST00000634840.1:c.1228-63_1228-37del	ENSP00000489324.1:n.1228-63_1228-37del
NM_005188.3:c.1228-63_1228-37del , LRG_608t1:c.1228-63_1228-37del	NP_005179.2:n.1228-63_1228-37del
XM_011543057.1:c.1228-63_1228-37del	XP_011541359.1:n.1228-63_1228-37del
NM_005188.4:c.1228-63_1228-37del MANE Select	NP_005179.2:n.1228-63_1228-37del