Canonical Allele Identifier: CA1919889815

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74070867_74070871delinsAGATT , CM000672.2:g.74070867_74070871delinsAGATT	GRCh38
NC_000010.10:g.75830625_75830629delinsAGATT , CM000672.1:g.75830625_75830629delinsAGATT	GRCh37
NC_000010.9:g.75500631_75500635delinsAGATT	NCBI36
NG_008868.1:g.77754_77758delinsAGATT , LRG_383:g.77754_77758delinsAGATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.390+47_390+51delinsAGATT MANE Select	ENSP00000211998.5:n.390+47_390+51delinsAGATT
ENST00000211998.8:c.390+47_390+51delinsAGATT	ENSP00000211998.4:n.390+47_390+51delinsAGATT
ENST00000372755.7:c.390+47_390+51delinsAGATT	ENSP00000361841.3:n.390+47_390+51delinsAGATT
ENST00000478896.2:n.331+27714_331+27718delinsAGATT
ENST00000623461.3:n.348+47_348+51delinsAGATT
ENST00000624354.3:c.*145+47_*145+51delinsAGATT	ENSP00000485551.1:n.*145+47_*145+51delinsAGATT
NM_003373.3:c.390+47_390+51delinsAGATT	NP_003364.1:n.390+47_390+51delinsAGATT
NM_014000.2:c.390+47_390+51delinsAGATT , LRG_383t1:c.390+47_390+51delinsAGATT	NP_054706.1:n.390+47_390+51delinsAGATT
XM_005270142.1:c.390+47_390+51delinsAGATT	XP_005270199.1:n.390+47_390+51delinsAGATT
XM_005270143.1:c.390+47_390+51delinsAGATT	XP_005270200.1:n.390+47_390+51delinsAGATT
NM_003373.4:c.390+47_390+51delinsAGATT	NP_003364.1:n.390+47_390+51delinsAGATT
NM_014000.3:c.390+47_390+51delinsAGATT MANE Select	NP_054706.1:n.390+47_390+51delinsAGATT