Canonical Allele Identifier: CA261764
Gene: VCL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.74074779dup , CM000672.2:g.74074779dup GRCh38
NC_000010.10:g.75834537dup , CM000672.1:g.75834537dup GRCh37
NC_000010.9:g.75504543dup NCBI36
NG_008868.1:g.81666dup , LRG_383:g.81666dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000211998.10:c.659dup MANE Select ENSP00000211998.5:p.Asn220LysfsTer21
ENST00000211998.8:c.659dup ENSP00000211998.4:p.Asn220LysfsTer21
ENST00000372755.7:c.659dup ENSP00000361841.3:p.Asn220LysfsTer21
ENST00000478896.2:n.332-26275dup
ENST00000623461.3:n.617dup
ENST00000624354.3:c.*414dup ENSP00000485551.1:n.*414dup
NM_003373.3:c.659dup NP_003364.1:p.Asn220LysfsTer21
NM_014000.2:c.659dup , LRG_383t1:c.659dup NP_054706.1:p.Asn220LysfsTer21
XM_005270142.1:c.659dup XP_005270199.1:p.Asn220LysfsTer21
XM_005270143.1:c.659dup XP_005270200.1:p.Asn220LysfsTer21
NM_003373.4:c.659dup NP_003364.1:p.Asn220LysfsTer21
NM_014000.3:c.659dup MANE Select NP_054706.1:p.Asn220LysfsTer21