Canonical Allele Identifier: CA1919890074

Gene: VCL

Linked Data

• dbSNP Id: rs1841658486

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74071173_74071175del , CM000672.2:g.74071173_74071175del	GRCh38
NC_000010.10:g.75830931_75830933del , CM000672.1:g.75830931_75830933del	GRCh37
NC_000010.9:g.75500937_75500939del	NCBI36
NG_008868.1:g.78060_78062del , LRG_383:g.78060_78062del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.499+90_499+92del MANE Select	ENSP00000211998.5:n.499+90_499+92del
ENST00000211998.8:c.499+90_499+92del	ENSP00000211998.4:n.499+90_499+92del
ENST00000372755.7:c.499+90_499+92del	ENSP00000361841.3:n.499+90_499+92del
ENST00000478896.2:n.331+28020_331+28022del
ENST00000623461.3:n.457+90_457+92del
ENST00000624354.3:c.*254+90_*254+92del	ENSP00000485551.1:n.*254+90_*254+92del
NM_003373.3:c.499+90_499+92del	NP_003364.1:n.499+90_499+92del
NM_014000.2:c.499+90_499+92del , LRG_383t1:c.499+90_499+92del	NP_054706.1:n.499+90_499+92del
XM_005270142.1:c.499+90_499+92del	XP_005270199.1:n.499+90_499+92del
XM_005270143.1:c.499+90_499+92del	XP_005270200.1:n.499+90_499+92del
NM_003373.4:c.499+90_499+92del	NP_003364.1:n.499+90_499+92del
NM_014000.3:c.499+90_499+92del MANE Select	NP_054706.1:n.499+90_499+92del