Canonical Allele Identifier: CA382911988
Gene: CBL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119277813C>T , CM000673.2:g.119277813C>T GRCh38
NC_000011.9:g.119148523C>T , CM000673.1:g.119148523C>T GRCh37
NC_000011.8:g.118653733C>T NCBI36
NG_016808.1:g.76534C>T , LRG_608:g.76534C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000700472.1:c.*516C>T ENSP00000515005.1:n.*516C>T
ENST00000264033.6:c.1064C>T MANE Select ENSP00000264033.3:p.Pro355Leu
ENST00000637974.1:c.1058C>T ENSP00000490763.1:p.Pro353Leu
ENST00000264033.5:c.1064C>T ENSP00000264033.3:p.Pro355Leu
ENST00000634586.1:c.1064C>T ENSP00000489218.1:p.Pro355Leu
ENST00000634840.1:c.1064C>T ENSP00000489324.1:p.Pro355Leu
NM_005188.3:c.1064C>T , LRG_608t1:c.1064C>T NP_005179.2:p.Pro355Leu
XM_011543057.1:c.1064C>T XP_011541359.1:p.Pro355Leu
NM_005188.4:c.1064C>T MANE Select NP_005179.2:p.Pro355Leu