Canonical Allele Identifier: CA5562872
Gene: VCL HGNC NCBI

Linked Data

dbSNP Id: rs750778483

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.74082497A>G , CM000672.2:g.74082497A>G GRCh38
NC_000010.10:g.75842255A>G , CM000672.1:g.75842255A>G GRCh37
NC_000010.9:g.75512261A>G NCBI36
NG_008868.1:g.89384A>G , LRG_383:g.89384A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000211998.10:c.827A>G MANE Select ENSP00000211998.5:p.Lys276Arg
ENST00000211998.8:c.827A>G ENSP00000211998.4:p.Lys276Arg
ENST00000372755.7:c.827A>G ENSP00000361841.3:p.Lys276Arg
ENST00000478896.2:n.332-18557A>G
ENST00000623461.3:n.3630A>G
ENST00000624354.3:c.*582A>G ENSP00000485551.1:n.*582A>G
NM_003373.3:c.827A>G NP_003364.1:p.Lys276Arg
NM_014000.2:c.827A>G , LRG_383t1:c.827A>G NP_054706.1:p.Lys276Arg
XM_005270142.1:c.830A>G XP_005270199.1:p.Lys277Arg
XM_005270143.1:c.830A>G XP_005270200.1:p.Lys277Arg
XR_001747501.1:n.90-4770T>C
NM_003373.4:c.827A>G NP_003364.1:p.Lys276Arg
NM_014000.3:c.827A>G MANE Select NP_054706.1:p.Lys276Arg