Canonical Allele Identifier: CA2575031950
Gene: CBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119278431T>C , CM000673.2:g.119278431T>C GRCh38
NC_000011.9:g.119149141T>C , CM000673.1:g.119149141T>C GRCh37
NC_000011.8:g.118654351T>C NCBI36
NG_016808.1:g.77152T>C , LRG_608:g.77152T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000700472.1:c.*680-79T>C ENSP00000515005.1:n.*680-79T>C
ENST00000264033.6:c.1228-79T>C MANE Select ENSP00000264033.3:n.1228-79T>C
ENST00000637974.1:c.1222-79T>C ENSP00000490763.1:n.1222-79T>C
ENST00000264033.5:c.1228-79T>C ENSP00000264033.3:n.1228-79T>C
ENST00000634586.1:c.1228-79T>C ENSP00000489218.1:n.1228-79T>C
ENST00000634840.1:c.1228-79T>C ENSP00000489324.1:n.1228-79T>C
NM_005188.3:c.1228-79T>C , LRG_608t1:c.1228-79T>C NP_005179.2:n.1228-79T>C
XM_011543057.1:c.1228-79T>C XP_011541359.1:n.1228-79T>C
NM_005188.4:c.1228-79T>C MANE Select NP_005179.2:n.1228-79T>C