Canonical Allele Identifier: CA2695199912
Gene: ACADVL HGNC NCBI

Linked Data

ClinVar Variation Id: 2680251
ClinVar RCV Id: RCV003460243

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221539_7221546del , CM000679.2:g.7221539_7221546del GRCh38
NC_000017.10:g.7124858_7124865del , CM000679.1:g.7124858_7124865del GRCh37
NC_000017.9:g.7065582_7065589del NCBI36
NG_007975.1:g.6706_6713del
NG_008391.2:g.3507_3514del

Transcript Alleles

HGVS Amino-acid change
ENST00000356839.10:c.479_486del
ENST00000322910.9:c.*434_*441del
ENST00000350303.9:c.413_420del
ENST00000356839.9:c.479_486del
ENST00000543245.6:c.548_555del
ENST00000577191.5:n.556_563del
ENST00000577433.5:n.687_694del
ENST00000577857.5:n.295_302del
ENST00000579286.5:n.660_667del
ENST00000579886.2:c.317_324del
ENST00000580365.1:n.210_217del
ENST00000581378.5:c.197_204del
ENST00000581562.5:n.525-413_525-406del
ENST00000582166.1:n.460_467del
ENST00000583312.5:c.479_486del
ENST00000583760.1:n.261_268del
NM_000018.3:c.479_486del
NM_001033859.2:c.413_420del
NM_001270447.1:c.548_555del
NM_001270448.1:c.251_258del
XM_006721516.2:c.479_486del
XM_011523829.1:c.479_486del
XM_011523830.1:c.479_486del
XR_934021.1:n.586_593del
XR_934022.1:n.586_593del
XR_934023.1:n.586_593del
XM_006721516.3:c.479_486del
XM_011523829.2:c.479_486del
XM_011523830.2:c.479_486del
XM_024450741.1:c.479_486del
XR_934021.2:n.538_545del
XR_934022.2:n.538_545del
XR_934023.2:n.538_545del
NM_000018.4:c.479_486del
NM_001033859.3:c.413_420del
NM_001270447.2:c.548_555del
NM_001270448.2:c.251_258del