Canonical Allele Identifier: CA1919908954

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74119597_74119600delinsCTTA , CM000672.2:g.74119597_74119600delinsCTTA	GRCh38
NC_000010.10:g.75879355_75879358delinsCTTA , CM000672.1:g.75879355_75879358delinsCTTA	GRCh37
NC_000010.9:g.75549361_75549364delinsCTTA	NCBI36
NG_008868.1:g.126484_126487delinsCTTA , LRG_383:g.126484_126487delinsCTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.*1428_*1431delinsCTTA MANE Select	ENSP00000211998.5:n.*1428_*1431delinsCTTA
ENST00000211998.8:c.*1428_*1431delinsCTTA	ENSP00000211998.4:n.*1428_*1431delinsCTTA
ENST00000372755.7:c.*1428_*1431delinsCTTA	ENSP00000361841.3:n.*1428_*1431delinsCTTA
ENST00000436396.1:c.3849_3852delinsCTTA	ENSP00000415489.1:n.3849_3852delinsCTTA
ENST00000623461.3:n.7432_7435delinsCTTA
NM_003373.3:c.*1428_*1431delinsCTTA	NP_003364.1:n.*1428_*1431delinsCTTA
NM_014000.2:c.*1428_*1431delinsCTTA , LRG_383t1:c.*1428_*1431delinsCTTA	NP_054706.1:n.*1428_*1431delinsCTTA
XM_005270142.1:c.*1428_*1431delinsCTTA	XP_005270199.1:n.*1428_*1431delinsCTTA
XM_005270143.1:c.*1428_*1431delinsCTTA	XP_005270200.1:n.*1428_*1431delinsCTTA
NM_003373.4:c.*1428_*1431delinsCTTA	NP_003364.1:n.*1428_*1431delinsCTTA
NM_014000.3:c.*1428_*1431delinsCTTA MANE Select	NP_054706.1:n.*1428_*1431delinsCTTA