Canonical Allele Identifier: CA668315493

Gene: VCL

Linked Data

• dbSNP Id: rs1319230058
• gnomAD v3: 10-74119431-AC-A
• gnomAD v4: 10-74119431-AC-A
• MyVariant Identifiers: chr10:g.75879190del (hg19) ; chr10:g.74119432del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74119433del , CM000672.2:g.74119433del	GRCh38
NC_000010.10:g.75879191del , CM000672.1:g.75879191del	GRCh37
NC_000010.9:g.75549197del	NCBI36
NG_008868.1:g.126320del , LRG_383:g.126320del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.*1264del MANE Select	ENSP00000211998.5:n.*1264del
ENST00000211998.8:c.*1264del	ENSP00000211998.4:n.*1264del
ENST00000372755.7:c.*1264del	ENSP00000361841.3:n.*1264del
ENST00000436396.1:c.3685del	ENSP00000415489.1:n.3685del
ENST00000623461.3:n.7268del
NM_003373.3:c.*1264del	NP_003364.1:n.*1264del
NM_014000.2:c.*1264del , LRG_383t1:c.*1264del	NP_054706.1:n.*1264del
XM_005270142.1:c.*1264del	XP_005270199.1:n.*1264del
XM_005270143.1:c.*1264del	XP_005270200.1:n.*1264del
NM_003373.4:c.*1264del	NP_003364.1:n.*1264del
NM_014000.3:c.*1264del MANE Select	NP_054706.1:n.*1264del