Canonical Allele Identifier: CA2842427060
Gene: VCL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.74111898dup , CM000672.2:g.74111898dup GRCh38
NC_000010.10:g.75871656dup , CM000672.1:g.75871656dup GRCh37
NC_000010.9:g.75541662dup NCBI36
NG_008868.1:g.118785dup , LRG_383:g.118785dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000211998.10:c.2746-11dup MANE Select ENSP00000211998.5:n.2746-11dup
ENST00000211998.8:c.2746-11dup ENSP00000211998.4:n.2746-11dup
ENST00000372755.7:c.2746-2286dup ENSP00000361841.3:n.2746-2286dup
ENST00000436396.1:c.1762-11dup ENSP00000415489.1:n.1762-11dup
ENST00000623461.3:n.5549-2286dup
ENST00000624354.3:c.*2501-11dup ENSP00000485551.1:n.*2501-11dup
NM_003373.3:c.2746-2286dup NP_003364.1:n.2746-2286dup
NM_014000.2:c.2746-11dup , LRG_383t1:c.2746-11dup NP_054706.1:n.2746-11dup
XM_005270142.1:c.2749-11dup XP_005270199.1:n.2749-11dup
XM_005270143.1:c.2749-2286dup XP_005270200.1:n.2749-2286dup
NM_003373.4:c.2746-2286dup NP_003364.1:n.2746-2286dup
NM_014000.3:c.2746-11dup MANE Select NP_054706.1:n.2746-11dup