Canonical Allele Identifier: CA668315624

Gene: VCL

Linked Data

• dbSNP Id: rs1052956679
• MyVariant Identifiers: chr10:g.75879358_75879359insTT (hg19) ; chr10:g.74119600_74119601insTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74119605_74119606dup , CM000672.2:g.74119605_74119606dup	GRCh38
NC_000010.10:g.75879363_75879364dup , CM000672.1:g.75879363_75879364dup	GRCh37
NC_000010.9:g.75549369_75549370dup	NCBI36
NG_008868.1:g.126492_126493dup , LRG_383:g.126492_126493dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.*1436_*1437dup MANE Select	ENSP00000211998.5:n.*1436_*1437dup
ENST00000211998.8:c.*1436_*1437dup	ENSP00000211998.4:n.*1436_*1437dup
ENST00000372755.7:c.*1436_*1437dup	ENSP00000361841.3:n.*1436_*1437dup
ENST00000436396.1:c.3857_3858dup	ENSP00000415489.1:n.3857_3858dup
ENST00000623461.3:n.7440_7441dup
NM_003373.3:c.*1436_*1437dup	NP_003364.1:n.*1436_*1437dup
NM_014000.2:c.*1436_*1437dup , LRG_383t1:c.*1436_*1437dup	NP_054706.1:n.*1436_*1437dup
XM_005270142.1:c.*1436_*1437dup	XP_005270199.1:n.*1436_*1437dup
XM_005270143.1:c.*1436_*1437dup	XP_005270200.1:n.*1436_*1437dup
NM_003373.4:c.*1436_*1437dup	NP_003364.1:n.*1436_*1437dup
NM_014000.3:c.*1436_*1437dup MANE Select	NP_054706.1:n.*1436_*1437dup