Canonical Allele Identifier: CA382911788

Gene: CBL

Linked Data

• gnomAD v4: 11-119277757-C-A
• MyVariant Identifiers: chr11:g.119148467C>A (hg19) ; chr11:g.119277757C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119277757C>A , CM000673.2:g.119277757C>A	GRCh38
NC_000011.9:g.119148467C>A , CM000673.1:g.119148467C>A	GRCh37
NC_000011.8:g.118653677C>A	NCBI36
NG_016808.1:g.76478C>A , LRG_608:g.76478C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700472.1:c.*460C>A	ENSP00000515005.1:n.*460C>A
ENST00000264033.6:c.1008C>A MANE Select	ENSP00000264033.3:p.Phe336Leu
ENST00000637974.1:c.1002C>A	ENSP00000490763.1:p.Phe334Leu
ENST00000264033.5:c.1008C>A	ENSP00000264033.3:p.Phe336Leu
ENST00000634586.1:c.1008C>A	ENSP00000489218.1:p.Phe336Leu
ENST00000634840.1:c.1008C>A	ENSP00000489324.1:p.Phe336Leu
NM_005188.3:c.1008C>A , LRG_608t1:c.1008C>A	NP_005179.2:p.Phe336Leu
XM_011543057.1:c.1008C>A	XP_011541359.1:p.Phe336Leu
NM_005188.4:c.1008C>A MANE Select	NP_005179.2:p.Phe336Leu