Canonical Allele Identifier: CA1919908955

Gene: VCL

Linked Data

• dbSNP Id: rs1840372721

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74119600_74119602del , CM000672.2:g.74119600_74119602del	GRCh38
NC_000010.10:g.75879358_75879360del , CM000672.1:g.75879358_75879360del	GRCh37
NC_000010.9:g.75549364_75549366del	NCBI36
NG_008868.1:g.126487_126489del , LRG_383:g.126487_126489del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.*1431_*1433del MANE Select	ENSP00000211998.5:n.*1431_*1433del
ENST00000211998.8:c.*1431_*1433del	ENSP00000211998.4:n.*1431_*1433del
ENST00000372755.7:c.*1431_*1433del	ENSP00000361841.3:n.*1431_*1433del
ENST00000436396.1:c.3852_3854del	ENSP00000415489.1:n.3852_3854del
ENST00000623461.3:n.7435_7437del
NM_003373.3:c.*1431_*1433del	NP_003364.1:n.*1431_*1433del
NM_014000.2:c.*1431_*1433del , LRG_383t1:c.*1431_*1433del	NP_054706.1:n.*1431_*1433del
XM_005270142.1:c.*1431_*1433del	XP_005270199.1:n.*1431_*1433del
XM_005270143.1:c.*1431_*1433del	XP_005270200.1:n.*1431_*1433del
NM_003373.4:c.*1431_*1433del	NP_003364.1:n.*1431_*1433del
NM_014000.3:c.*1431_*1433del MANE Select	NP_054706.1:n.*1431_*1433del