Canonical Allele Identifier: CA2835624428

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74082551del , CM000672.2:g.74082551del	GRCh38
NC_000010.10:g.75842309del , CM000672.1:g.75842309del	GRCh37
NC_000010.9:g.75512315del	NCBI36
NG_008868.1:g.89438del , LRG_383:g.89438del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.874+7del MANE Select	ENSP00000211998.5:n.874+7del
ENST00000211998.8:c.874+7del	ENSP00000211998.4:n.874+7del
ENST00000372755.7:c.874+7del	ENSP00000361841.3:n.874+7del
ENST00000478896.2:n.332-18503del
ENST00000623461.3:n.3677+7del
ENST00000624354.3:c.*629+7del	ENSP00000485551.1:n.*629+7del
NM_003373.3:c.874+7del	NP_003364.1:n.874+7del
NM_014000.2:c.874+7del , LRG_383t1:c.874+7del	NP_054706.1:n.874+7del
XM_005270142.1:c.877+7del	XP_005270199.1:n.877+7del
XM_005270143.1:c.877+7del	XP_005270200.1:n.877+7del
XR_001747501.1:n.90-4822del
NM_003373.4:c.874+7del	NP_003364.1:n.874+7del
NM_014000.3:c.874+7del MANE Select	NP_054706.1:n.874+7del