Canonical Allele Identifier: CA2788548333

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74070960_74070961del , CM000672.2:g.74070960_74070961del	GRCh38
NC_000010.10:g.75830718_75830719del , CM000672.1:g.75830718_75830719del	GRCh37
NC_000010.9:g.75500724_75500725del	NCBI36
NG_008868.1:g.77847_77848del , LRG_383:g.77847_77848del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.391-15_391-14del MANE Select	ENSP00000211998.5:n.391-15_391-14del
ENST00000211998.8:c.391-15_391-14del	ENSP00000211998.4:n.391-15_391-14del
ENST00000372755.7:c.391-15_391-14del	ENSP00000361841.3:n.391-15_391-14del
ENST00000478896.2:n.331+27807_331+27808del
ENST00000623461.3:n.349-15_349-14del
ENST00000624354.3:c.*146-15_*146-14del	ENSP00000485551.1:n.*146-15_*146-14del
NM_003373.3:c.391-15_391-14del	NP_003364.1:n.391-15_391-14del
NM_014000.2:c.391-15_391-14del , LRG_383t1:c.391-15_391-14del	NP_054706.1:n.391-15_391-14del
XM_005270142.1:c.391-15_391-14del	XP_005270199.1:n.391-15_391-14del
XM_005270143.1:c.391-15_391-14del	XP_005270200.1:n.391-15_391-14del
NM_003373.4:c.391-15_391-14del	NP_003364.1:n.391-15_391-14del
NM_014000.3:c.391-15_391-14del MANE Select	NP_054706.1:n.391-15_391-14del