Canonical Allele Identifier: CA382912922

Gene: CBL

Linked Data

• dbSNP Id: rs2135303916
• MyVariant Identifiers: chr11:g.119149004G>A (hg19) ; chr11:g.119278294G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119278294G>A , CM000673.2:g.119278294G>A	GRCh38
NC_000011.9:g.119149004G>A , CM000673.1:g.119149004G>A	GRCh37
NC_000011.8:g.118654214G>A	NCBI36
NG_016808.1:g.77015G>A , LRG_608:g.77015G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700472.1:c.*676G>A	ENSP00000515005.1:n.*676G>A
ENST00000264033.6:c.1224G>A MANE Select	ENSP00000264033.3:p.Trp408Ter
ENST00000637974.1:c.1218G>A	ENSP00000490763.1:p.Trp406Ter
ENST00000264033.5:c.1224G>A	ENSP00000264033.3:p.Trp408Ter
ENST00000634586.1:c.1224G>A	ENSP00000489218.1:p.Trp408Ter
ENST00000634840.1:c.1224G>A	ENSP00000489324.1:p.Trp408Ter
NM_005188.3:c.1224G>A , LRG_608t1:c.1224G>A	NP_005179.2:p.Trp408Ter
XM_011543057.1:c.1224G>A	XP_011541359.1:p.Trp408Ter
NM_005188.4:c.1224G>A MANE Select	NP_005179.2:p.Trp408Ter