Canonical Allele Identifier: CA2793839085
Gene: CBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119278362G>C , CM000673.2:g.119278362G>C GRCh38
NC_000011.9:g.119149072G>C , CM000673.1:g.119149072G>C GRCh37
NC_000011.8:g.118654282G>C NCBI36
NG_016808.1:g.77083G>C , LRG_608:g.77083G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000700472.1:c.*679+65G>C ENSP00000515005.1:n.*679+65G>C
ENST00000264033.6:c.1227+65G>C MANE Select ENSP00000264033.3:n.1227+65G>C
ENST00000637974.1:c.1221+65G>C ENSP00000490763.1:n.1221+65G>C
ENST00000264033.5:c.1227+65G>C ENSP00000264033.3:n.1227+65G>C
ENST00000634586.1:c.1227+65G>C ENSP00000489218.1:n.1227+65G>C
ENST00000634840.1:c.1227+65G>C ENSP00000489324.1:n.1227+65G>C
NM_005188.3:c.1227+65G>C , LRG_608t1:c.1227+65G>C NP_005179.2:n.1227+65G>C
XM_011543057.1:c.1227+65G>C XP_011541359.1:n.1227+65G>C
NM_005188.4:c.1227+65G>C MANE Select NP_005179.2:n.1227+65G>C