Canonical Allele Identifier: CA2609715437

Gene: VCL

Linked Data

• gnomAD v4: 10-74070960-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74070963del , CM000672.2:g.74070963del	GRCh38
NC_000010.10:g.75830721del , CM000672.1:g.75830721del	GRCh37
NC_000010.9:g.75500727del	NCBI36
NG_008868.1:g.77850del , LRG_383:g.77850del

Transcript Alleles

HGVS	Amino-acid change
ENST00000211998.10:c.391-12del MANE Select	ENSP00000211998.5:n.391-12del
ENST00000211998.8:c.391-12del	ENSP00000211998.4:n.391-12del
ENST00000372755.7:c.391-12del	ENSP00000361841.3:n.391-12del
ENST00000478896.2:n.331+27810del
ENST00000623461.3:n.349-12del
ENST00000624354.3:c.*146-12del	ENSP00000485551.1:n.*146-12del
NM_003373.3:c.391-12del	NP_003364.1:n.391-12del
NM_014000.2:c.391-12del , LRG_383t1:c.391-12del	NP_054706.1:n.391-12del
XM_005270142.1:c.391-12del	XP_005270199.1:n.391-12del
XM_005270143.1:c.391-12del	XP_005270200.1:n.391-12del
NM_003373.4:c.391-12del	NP_003364.1:n.391-12del
NM_014000.3:c.391-12del MANE Select	NP_054706.1:n.391-12del