Canonical Allele Identifier: CA2609730644
Gene: VCL HGNC NCBI

Linked Data

gnomAD v4: 10-74119498-AT-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.74119501del , CM000672.2:g.74119501del GRCh38
NC_000010.10:g.75879259del , CM000672.1:g.75879259del GRCh37
NC_000010.9:g.75549265del NCBI36
NG_008868.1:g.126388del , LRG_383:g.126388del

Transcript Alleles

HGVS Amino-acid change
ENST00000211998.10:c.*1332del MANE Select ENSP00000211998.5:n.*1332del
ENST00000211998.8:c.*1332del ENSP00000211998.4:n.*1332del
ENST00000372755.7:c.*1332del ENSP00000361841.3:n.*1332del
ENST00000436396.1:c.3753del ENSP00000415489.1:n.3753del
ENST00000623461.3:n.7336del
NM_003373.3:c.*1332del NP_003364.1:n.*1332del
NM_014000.2:c.*1332del , LRG_383t1:c.*1332del NP_054706.1:n.*1332del
XM_005270142.1:c.*1332del XP_005270199.1:n.*1332del
XM_005270143.1:c.*1332del XP_005270200.1:n.*1332del
NM_003373.4:c.*1332del NP_003364.1:n.*1332del
NM_014000.3:c.*1332del MANE Select NP_054706.1:n.*1332del
Search 100 bp 5'
Search 100 bp 3'