Canonical Allele Identifier: CA382975756
Gene: CBL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119206455G>C , CM000673.2:g.119206455G>C GRCh38
NC_000011.9:g.119077165G>C , CM000673.1:g.119077165G>C GRCh37
NC_000011.8:g.118582375G>C NCBI36
NG_016808.1:g.5176G>C , LRG_608:g.5176G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000700472.1:c.38G>C ENSP00000515005.1:p.Gly13Ala
ENST00000264033.6:c.38G>C MANE Select ENSP00000264033.3:p.Gly13Ala
ENST00000637974.1:c.32G>C ENSP00000490763.1:p.Gly11Ala
ENST00000264033.5:c.38G>C ENSP00000264033.3:p.Gly13Ala
ENST00000634586.1:c.38G>C ENSP00000489218.1:p.Gly13Ala
ENST00000634840.1:c.38G>C ENSP00000489324.1:p.Gly13Ala
NM_005188.3:c.38G>C , LRG_608t1:c.38G>C NP_005179.2:p.Gly13Ala
XM_011543057.1:c.38G>C XP_011541359.1:p.Gly13Ala
NM_005188.4:c.38G>C MANE Select NP_005179.2:p.Gly13Ala