Canonical Allele Identifier: CA16041874
Gene: ACADVL HGNC NCBI

Linked Data

ClinVar Variation Id: 371516
ClinVar RCV Id: RCV000409489
dbSNP Id: rs1057517331

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223990dup , CM000679.2:g.7223990dup GRCh38
NC_000017.10:g.7127309dup , CM000679.1:g.7127309dup GRCh37
NC_000017.9:g.7068033dup NCBI36
NG_007975.1:g.9157dup
NG_008391.2:g.1061dup
NG_033038.1:g.15555dup

Transcript Alleles

HGVS Amino-acid change
ENST00000356839.10:c.1355dup MANE Select ENSP00000349297.5:p.Arg453ProfsTer10
ENST00000322910.9:c.*1310dup ENSP00000325395.5:n.*1310dup
ENST00000350303.9:c.1289dup ENSP00000344152.5:p.Arg431ProfsTer10
ENST00000356839.9:c.1355dup ENSP00000349297.5:p.Arg453ProfsTer10
ENST00000542255.6:c.213dup
ENST00000543245.6:c.1424dup ENSP00000438689.2:p.Arg476ProfsTer10
ENST00000578711.1:n.486dup
ENST00000579425.5:n.471dup
ENST00000579546.1:c.192dup
ENST00000579894.5:n.66dup
ENST00000583074.5:n.74dup
ENST00000583850.5:n.130dup
ENST00000583858.5:c.384dup
ENST00000585203.6:n.546dup
NM_000018.3:c.1355dup NP_000009.1:p.Arg453ProfsTer10
NM_001033859.2:c.1289dup NP_001029031.1:p.Arg431ProfsTer10
NM_001270447.1:c.1424dup NP_001257376.1:p.Arg476ProfsTer10
NM_001270448.1:c.1127dup NP_001257377.1:p.Arg377ProfsTer10
XM_006721516.2:c.1355dup XP_006721579.2:p.Arg453ProfsTer10
XM_011523829.1:c.1355dup XP_011522131.1:p.Arg453ProfsTer10
XM_011523830.1:c.1355dup XP_011522132.1:p.Arg453ProfsTer10
XR_934021.1:n.1462dup
XR_934022.1:n.1462dup
XR_934023.1:n.1462dup
XM_006721516.3:c.1355dup XP_006721579.2:p.Arg453ProfsTer10
XM_011523829.2:c.1355dup XP_011522131.1:p.Arg453ProfsTer10
XM_011523830.2:c.1355dup XP_011522132.1:p.Arg453ProfsTer10
XM_024450741.1:c.1355dup XP_024306509.1:p.Arg453ProfsTer10
XR_934021.2:n.1414dup
XR_934022.2:n.1414dup
XR_934023.2:n.1414dup
NM_000018.4:c.1355dup MANE Select NP_000009.1:p.Arg453ProfsTer10
NM_001033859.3:c.1289dup NP_001029031.1:p.Arg431ProfsTer10
NM_001270447.2:c.1424dup NP_001257376.1:p.Arg476ProfsTer10
NM_001270448.2:c.1127dup NP_001257377.1:p.Arg377ProfsTer10