Canonical Allele Identifier: CA382912006
Gene: CBL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119277818C>A , CM000673.2:g.119277818C>A GRCh38
NC_000011.9:g.119148528C>A , CM000673.1:g.119148528C>A GRCh37
NC_000011.8:g.118653738C>A NCBI36
NG_016808.1:g.76539C>A , LRG_608:g.76539C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000700472.1:c.*521C>A ENSP00000515005.1:n.*521C>A
ENST00000264033.6:c.1069C>A MANE Select ENSP00000264033.3:p.Pro357Thr
ENST00000637974.1:c.1063C>A ENSP00000490763.1:p.Pro355Thr
ENST00000264033.5:c.1069C>A ENSP00000264033.3:p.Pro357Thr
ENST00000634586.1:c.1069C>A ENSP00000489218.1:p.Pro357Thr
ENST00000634840.1:c.1069C>A ENSP00000489324.1:p.Pro357Thr
NM_005188.3:c.1069C>A , LRG_608t1:c.1069C>A NP_005179.2:p.Pro357Thr
XM_011543057.1:c.1069C>A XP_011541359.1:p.Pro357Thr
NM_005188.4:c.1069C>A MANE Select NP_005179.2:p.Pro357Thr