Canonical Allele Identifier: CA377266823
Gene: VCL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.74071072A>C , CM000672.2:g.74071072A>C GRCh38
NC_000010.10:g.75830830A>C , CM000672.1:g.75830830A>C GRCh37
NC_000010.9:g.75500836A>C NCBI36
NG_008868.1:g.77959A>C , LRG_383:g.77959A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000211998.10:c.488A>C MANE Select ENSP00000211998.5:p.Asn163Thr
ENST00000211998.8:c.488A>C ENSP00000211998.4:p.Asn163Thr
ENST00000372755.7:c.488A>C ENSP00000361841.3:p.Asn163Thr
ENST00000478896.2:n.331+27919A>C
ENST00000623461.3:n.446A>C
ENST00000624354.3:c.*243A>C ENSP00000485551.1:n.*243A>C
NM_003373.3:c.488A>C NP_003364.1:p.Asn163Thr
NM_014000.2:c.488A>C , LRG_383t1:c.488A>C NP_054706.1:p.Asn163Thr
XM_005270142.1:c.488A>C XP_005270199.1:p.Asn163Thr
XM_005270143.1:c.488A>C XP_005270200.1:p.Asn163Thr
NM_003373.4:c.488A>C NP_003364.1:p.Asn163Thr
NM_014000.3:c.488A>C MANE Select NP_054706.1:p.Asn163Thr