Canonical Allele Identifier: CA1919889886
Gene: VCL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.74070949T= , CM000672.2:g.74070949T= GRCh38
NC_000010.10:g.75830707T= , CM000672.1:g.75830707T= GRCh37
NC_000010.9:g.75500713T= NCBI36
NG_008868.1:g.77836T= , LRG_383:g.77836T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000211998.10:c.391-26T= MANE Select ENSP00000211998.5:n.391-26T=
ENST00000211998.8:c.391-26T= ENSP00000211998.4:n.391-26T=
ENST00000372755.7:c.391-26T= ENSP00000361841.3:n.391-26T=
ENST00000478896.2:n.331+27796T=
ENST00000623461.3:n.349-26T=
ENST00000624354.3:c.*146-26T= ENSP00000485551.1:n.*146-26T=
NM_003373.3:c.391-26T= NP_003364.1:n.391-26T=
NM_014000.2:c.391-26T= , LRG_383t1:c.391-26T= NP_054706.1:n.391-26T=
XM_005270142.1:c.391-26T= XP_005270199.1:n.391-26T=
XM_005270143.1:c.391-26T= XP_005270200.1:n.391-26T=
NM_003373.4:c.391-26T= NP_003364.1:n.391-26T=
NM_014000.3:c.391-26T= MANE Select NP_054706.1:n.391-26T=