Canonical Allele Identifier: CA382912036
Gene: CBL HGNC NCBI

Linked Data

dbSNP Id: rs1341984560

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119277824G>A , CM000673.2:g.119277824G>A GRCh38
NC_000011.9:g.119148534G>A , CM000673.1:g.119148534G>A GRCh37
NC_000011.8:g.118653744G>A NCBI36
NG_016808.1:g.76545G>A , LRG_608:g.76545G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000700472.1:c.*527G>A ENSP00000515005.1:n.*527G>A
ENST00000264033.6:c.1075G>A MANE Select ENSP00000264033.3:p.Asp359Asn
ENST00000637974.1:c.1069G>A ENSP00000490763.1:p.Asp357Asn
ENST00000264033.5:c.1075G>A ENSP00000264033.3:p.Asp359Asn
ENST00000634586.1:c.1075G>A ENSP00000489218.1:p.Asp359Asn
ENST00000634840.1:c.1075G>A ENSP00000489324.1:p.Asp359Asn
NM_005188.3:c.1075G>A , LRG_608t1:c.1075G>A NP_005179.2:p.Asp359Asn
XM_011543057.1:c.1075G>A XP_011541359.1:p.Asp359Asn
NM_005188.4:c.1075G>A MANE Select NP_005179.2:p.Asp359Asn