Canonical Allele Identifier: CA282018
Gene: CBL HGNC NCBI

Linked Data

ClinVar Variation Id: 40404
ClinVar RCV Id: RCV000033351
dbSNP Id: rs397507490

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119277825_119277836del , CM000673.2:g.119277825_119277836del GRCh38
NC_000011.9:g.119148535_119148546del , CM000673.1:g.119148535_119148546del GRCh37
NC_000011.8:g.118653745_118653756del NCBI36
NG_016808.1:g.76546_76557del , LRG_608:g.76546_76557del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700472.1:c.*528_*539del ENSP00000515005.1:n.*528_*539del
ENST00000264033.6:c.1076_1087del MANE Select ENSP00000264033.3:p.Asp359_Lys362del
ENST00000637974.1:c.1070_1081del ENSP00000490763.1:p.Asp357_Lys360del
ENST00000264033.5:c.1076_1087del ENSP00000264033.3:p.Asp359_Lys362del
ENST00000634586.1:c.1076_1087del ENSP00000489218.1:p.Asp359_Lys362del
ENST00000634840.1:c.1076_1087del ENSP00000489324.1:p.Asp359_Lys362del
NM_005188.3:c.1076_1087del , LRG_608t1:c.1076_1087del NP_005179.2:p.Asp359_Lys362del
XM_011543057.1:c.1076_1087del XP_011541359.1:p.Asp359_Lys362del
NM_005188.4:c.1076_1087del MANE Select NP_005179.2:p.Asp359_Lys362del