Canonical Allele Identifier: CA382912702

Gene: CBL

Linked Data

• dbSNP Id: rs2135303809
• COSMIC: COSM97084
• MyVariant Identifiers: chr11:g.119148963C>G (hg19) ; chr11:g.119278253C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119278253C>G , CM000673.2:g.119278253C>G	GRCh38
NC_000011.9:g.119148963C>G , CM000673.1:g.119148963C>G	GRCh37
NC_000011.8:g.118654173C>G	NCBI36
NG_016808.1:g.76974C>G , LRG_608:g.76974C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700472.1:c.*635C>G	ENSP00000515005.1:n.*635C>G
ENST00000264033.6:c.1183C>G MANE Select	ENSP00000264033.3:p.Pro395Ala
ENST00000637974.1:c.1177C>G	ENSP00000490763.1:p.Pro393Ala
ENST00000264033.5:c.1183C>G	ENSP00000264033.3:p.Pro395Ala
ENST00000634586.1:c.1183C>G	ENSP00000489218.1:p.Pro395Ala
ENST00000634840.1:c.1183C>G	ENSP00000489324.1:p.Pro395Ala
NM_005188.3:c.1183C>G , LRG_608t1:c.1183C>G	NP_005179.2:p.Pro395Ala
XM_011543057.1:c.1183C>G	XP_011541359.1:p.Pro395Ala
NM_005188.4:c.1183C>G MANE Select	NP_005179.2:p.Pro395Ala