Canonical Allele Identifier: CA1919890027

Gene: VCL

Linked Data

• dbSNP Id: rs1841657036

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74071087_74071088insT , CM000672.2:g.74071087_74071088insT	GRCh38
NC_000010.10:g.75830845_75830846insT , CM000672.1:g.75830845_75830846insT	GRCh37
NC_000010.9:g.75500851_75500852insT	NCBI36
NG_008868.1:g.77974_77975insT , LRG_383:g.77974_77975insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.499+4_499+5insT MANE Select	ENSP00000211998.5:n.499+4_499+5insT
ENST00000211998.8:c.499+4_499+5insT	ENSP00000211998.4:n.499+4_499+5insT
ENST00000372755.7:c.499+4_499+5insT	ENSP00000361841.3:n.499+4_499+5insT
ENST00000478896.2:n.331+27934_331+27935insT
ENST00000623461.3:n.457+4_457+5insT
ENST00000624354.3:c.*254+4_*254+5insT	ENSP00000485551.1:n.*254+4_*254+5insT
NM_003373.3:c.499+4_499+5insT	NP_003364.1:n.499+4_499+5insT
NM_014000.2:c.499+4_499+5insT , LRG_383t1:c.499+4_499+5insT	NP_054706.1:n.499+4_499+5insT
XM_005270142.1:c.499+4_499+5insT	XP_005270199.1:n.499+4_499+5insT
XM_005270143.1:c.499+4_499+5insT	XP_005270200.1:n.499+4_499+5insT
NM_003373.4:c.499+4_499+5insT	NP_003364.1:n.499+4_499+5insT
NM_014000.3:c.499+4_499+5insT MANE Select	NP_054706.1:n.499+4_499+5insT