Canonical Allele Identifier: CA2580094810
Gene: ACADVL HGNC NCBI

Linked Data

ClinVar Variation Id: 2069131
ClinVar RCV Id: RCV002961922

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224084dup , CM000679.2:g.7224084dup GRCh38
NC_000017.10:g.7127403dup , CM000679.1:g.7127403dup GRCh37
NC_000017.9:g.7068127dup NCBI36
NG_007975.1:g.9251dup
NG_008391.2:g.968dup
NG_033038.1:g.15462dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1434+15dup MANE Select ENSP00000349297.5:n.1434+15dup
ENST00000322910.9:c.*1389+15dup ENSP00000325395.5:n.*1389+15dup
ENST00000350303.9:c.1368+15dup ENSP00000344152.5:n.1368+15dup
ENST00000356839.9:c.1434+15dup ENSP00000349297.5:n.1434+15dup
ENST00000542255.6:c.292+15dup
ENST00000543245.6:c.1503+15dup ENSP00000438689.2:n.1503+15dup
ENST00000578711.1:n.580dup
ENST00000579425.5:n.550+15dup
ENST00000579546.1:c.271+15dup
ENST00000579894.5:n.160dup
ENST00000583074.5:n.153+15dup
ENST00000583850.5:n.209+15dup
ENST00000583858.5:c.463+15dup
ENST00000585203.6:n.625+15dup
NM_000018.3:c.1434+15dup NP_000009.1:n.1434+15dup
NM_001033859.2:c.1368+15dup NP_001029031.1:n.1368+15dup
NM_001270447.1:c.1503+15dup NP_001257376.1:n.1503+15dup
NM_001270448.1:c.1206+15dup NP_001257377.1:n.1206+15dup
XM_006721516.2:c.1434+15dup XP_006721579.2:n.1434+15dup
XM_011523829.1:c.1434+15dup XP_011522131.1:n.1434+15dup
XM_011523830.1:c.1434+15dup XP_011522132.1:n.1434+15dup
XR_934021.1:n.1541+15dup
XR_934022.1:n.1541+15dup
XR_934023.1:n.1541+15dup
XM_006721516.3:c.1434+15dup XP_006721579.2:n.1434+15dup
XM_011523829.2:c.1434+15dup XP_011522131.1:n.1434+15dup
XM_011523830.2:c.1434+15dup XP_011522132.1:n.1434+15dup
XM_024450741.1:c.1434+15dup XP_024306509.1:n.1434+15dup
XR_934021.2:n.1493+15dup
XR_934022.2:n.1493+15dup
XR_934023.2:n.1493+15dup
NM_000018.4:c.1434+15dup MANE Select NP_000009.1:n.1434+15dup
NM_001033859.3:c.1368+15dup NP_001029031.1:n.1368+15dup
NM_001270447.2:c.1503+15dup NP_001257376.1:n.1503+15dup
NM_001270448.2:c.1206+15dup NP_001257377.1:n.1206+15dup