Canonical Allele Identifier: CA774743623
Gene: ACADVL HGNC NCBI

Linked Data

ClinVar Variation Id: 932850
ClinVar RCV Id: RCV001200807
dbSNP Id: rs1402646371

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222847_7222848del , CM000679.2:g.7222847_7222848del GRCh38
NC_000017.10:g.7126166_7126167del , CM000679.1:g.7126166_7126167del GRCh37
NC_000017.9:g.7066890_7066891del NCBI36
NG_007975.1:g.8014_8015del
NG_008391.2:g.2206_2207del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1059_1060del MANE Select ENSP00000349297.5:p.Gly354HisfsTer4
ENST00000322910.9:c.*1014_*1015del ENSP00000325395.5:n.*1014_*1015del
ENST00000350303.9:c.993_994del ENSP00000344152.5:p.Gly332HisfsTer4
ENST00000356839.9:c.1059_1060del ENSP00000349297.5:p.Gly354HisfsTer4
ENST00000543245.6:c.1128_1129del ENSP00000438689.2:p.Gly377HisfsTer4
ENST00000578824.5:n.208_209del
ENST00000582379.1:n.443_444del
ENST00000583858.5:c.88_89del
NM_000018.3:c.1059_1060del NP_000009.1:p.Gly354HisfsTer4
NM_001033859.2:c.993_994del NP_001029031.1:p.Gly332HisfsTer4
NM_001270447.1:c.1128_1129del NP_001257376.1:p.Gly377HisfsTer4
NM_001270448.1:c.831_832del NP_001257377.1:p.Gly278HisfsTer4
XM_006721516.2:c.1059_1060del XP_006721579.2:p.Gly354HisfsTer4
XM_011523829.1:c.1059_1060del XP_011522131.1:p.Gly354HisfsTer4
XM_011523830.1:c.1059_1060del XP_011522132.1:p.Gly354HisfsTer4
XR_934021.1:n.1166_1167del
XR_934022.1:n.1166_1167del
XR_934023.1:n.1166_1167del
XM_006721516.3:c.1059_1060del XP_006721579.2:p.Gly354HisfsTer4
XM_011523829.2:c.1059_1060del XP_011522131.1:p.Gly354HisfsTer4
XM_011523830.2:c.1059_1060del XP_011522132.1:p.Gly354HisfsTer4
XM_024450741.1:c.1059_1060del XP_024306509.1:p.Gly354HisfsTer4
XR_934021.2:n.1118_1119del
XR_934022.2:n.1118_1119del
XR_934023.2:n.1118_1119del
NM_000018.4:c.1059_1060del MANE Select NP_000009.1:p.Gly354HisfsTer4
NM_001033859.3:c.993_994del NP_001029031.1:p.Gly332HisfsTer4
NM_001270447.2:c.1128_1129del NP_001257376.1:p.Gly377HisfsTer4
NM_001270448.2:c.831_832del NP_001257377.1:p.Gly278HisfsTer4