Canonical Allele Identifier: CA2574585373
Gene: VCL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.74071167dup , CM000672.2:g.74071167dup GRCh38
NC_000010.10:g.75830925dup , CM000672.1:g.75830925dup GRCh37
NC_000010.9:g.75500931dup NCBI36
NG_008868.1:g.78054dup , LRG_383:g.78054dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000211998.10:c.499+84dup MANE Select ENSP00000211998.5:n.499+84dup
ENST00000211998.8:c.499+84dup ENSP00000211998.4:n.499+84dup
ENST00000372755.7:c.499+84dup ENSP00000361841.3:n.499+84dup
ENST00000478896.2:n.331+28014dup
ENST00000623461.3:n.457+84dup
ENST00000624354.3:c.*254+84dup ENSP00000485551.1:n.*254+84dup
NM_003373.3:c.499+84dup NP_003364.1:n.499+84dup
NM_014000.2:c.499+84dup , LRG_383t1:c.499+84dup NP_054706.1:n.499+84dup
XM_005270142.1:c.499+84dup XP_005270199.1:n.499+84dup
XM_005270143.1:c.499+84dup XP_005270200.1:n.499+84dup
NM_003373.4:c.499+84dup NP_003364.1:n.499+84dup
NM_014000.3:c.499+84dup MANE Select NP_054706.1:n.499+84dup