Canonical Allele Identifier: CA1919908958
Gene: VCL HGNC NCBI

Linked Data

dbSNP Id: rs1052956679
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.74119606dup , CM000672.2:g.74119606dup GRCh38
NC_000010.10:g.75879364dup , CM000672.1:g.75879364dup GRCh37
NC_000010.9:g.75549370dup NCBI36
NG_008868.1:g.126493dup , LRG_383:g.126493dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000211998.10:c.*1437dup MANE Select ENSP00000211998.5:n.*1437dup
ENST00000211998.8:c.*1437dup ENSP00000211998.4:n.*1437dup
ENST00000372755.7:c.*1437dup ENSP00000361841.3:n.*1437dup
ENST00000436396.1:c.3858dup ENSP00000415489.1:n.3858dup
ENST00000623461.3:n.7441dup
NM_003373.3:c.*1437dup NP_003364.1:n.*1437dup
NM_014000.2:c.*1437dup , LRG_383t1:c.*1437dup NP_054706.1:n.*1437dup
XM_005270142.1:c.*1437dup XP_005270199.1:n.*1437dup
XM_005270143.1:c.*1437dup XP_005270200.1:n.*1437dup
NM_003373.4:c.*1437dup NP_003364.1:n.*1437dup
NM_014000.3:c.*1437dup MANE Select NP_054706.1:n.*1437dup
Search 100 bp 5'
Search 100 bp 3'