Canonical Allele Identifier: CA382912106

Gene: CBL

Linked Data

• ClinVar Variation Id: 1334228
• ClinVar RCV Id: RCV001813643 ; RCV002541488
• dbSNP Id: rs2135303015
• gnomAD v4: 11-119277840-C-T
• MyVariant Identifiers: chr11:g.119148550C>T (hg19) ; chr11:g.119277840C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119277840C>T , CM000673.2:g.119277840C>T	GRCh38
NC_000011.9:g.119148550C>T , CM000673.1:g.119148550C>T	GRCh37
NC_000011.8:g.118653760C>T	NCBI36
NG_016808.1:g.76561C>T , LRG_608:g.76561C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700472.1:c.*543C>T	ENSP00000515005.1:n.*543C>T
ENST00000264033.6:c.1091C>T MANE Select	ENSP00000264033.3:p.Thr364Ile
ENST00000637974.1:c.1085C>T	ENSP00000490763.1:p.Thr362Ile
ENST00000264033.5:c.1091C>T	ENSP00000264033.3:p.Thr364Ile
ENST00000634586.1:c.1091C>T	ENSP00000489218.1:p.Thr364Ile
ENST00000634840.1:c.1091C>T	ENSP00000489324.1:p.Thr364Ile
NM_005188.3:c.1091C>T , LRG_608t1:c.1091C>T	NP_005179.2:p.Thr364Ile
XM_011543057.1:c.1091C>T	XP_011541359.1:p.Thr364Ile
NM_005188.4:c.1091C>T MANE Select	NP_005179.2:p.Thr364Ile