Canonical Allele Identifier: CA2788548335
Gene: VCL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.74070971del , CM000672.2:g.74070971del GRCh38
NC_000010.10:g.75830729del , CM000672.1:g.75830729del GRCh37
NC_000010.9:g.75500735del NCBI36
NG_008868.1:g.77858del , LRG_383:g.77858del

Transcript Alleles

HGVS Amino-acid Change
ENST00000211998.10:c.391-4del MANE Select ENSP00000211998.5:n.391-4del
ENST00000211998.8:c.391-4del ENSP00000211998.4:n.391-4del
ENST00000372755.7:c.391-4del ENSP00000361841.3:n.391-4del
ENST00000478896.2:n.331+27818del
ENST00000623461.3:n.349-4del
ENST00000624354.3:c.*146-4del ENSP00000485551.1:n.*146-4del
NM_003373.3:c.391-4del NP_003364.1:n.391-4del
NM_014000.2:c.391-4del , LRG_383t1:c.391-4del NP_054706.1:n.391-4del
XM_005270142.1:c.391-4del XP_005270199.1:n.391-4del
XM_005270143.1:c.391-4del XP_005270200.1:n.391-4del
NM_003373.4:c.391-4del NP_003364.1:n.391-4del
NM_014000.3:c.391-4del MANE Select NP_054706.1:n.391-4del
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