Canonical Allele Identifier: CA2609715552

Gene: VCL

Linked Data

• gnomAD v4: 10-74071162-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74071167del , CM000672.2:g.74071167del	GRCh38
NC_000010.10:g.75830925del , CM000672.1:g.75830925del	GRCh37
NC_000010.9:g.75500931del	NCBI36
NG_008868.1:g.78054del , LRG_383:g.78054del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.499+84del MANE Select	ENSP00000211998.5:n.499+84del
ENST00000211998.8:c.499+84del	ENSP00000211998.4:n.499+84del
ENST00000372755.7:c.499+84del	ENSP00000361841.3:n.499+84del
ENST00000478896.2:n.331+28014del
ENST00000623461.3:n.457+84del
ENST00000624354.3:c.*254+84del	ENSP00000485551.1:n.*254+84del
NM_003373.3:c.499+84del	NP_003364.1:n.499+84del
NM_014000.2:c.499+84del , LRG_383t1:c.499+84del	NP_054706.1:n.499+84del
XM_005270142.1:c.499+84del	XP_005270199.1:n.499+84del
XM_005270143.1:c.499+84del	XP_005270200.1:n.499+84del
NM_003373.4:c.499+84del	NP_003364.1:n.499+84del
NM_014000.3:c.499+84del MANE Select	NP_054706.1:n.499+84del