Canonical Allele Identifier: CA287440583
Gene: ACADVL HGNC NCBI

Linked Data

ClinVar Variation Id: 932813
ClinVar RCV Id: RCV001200764
dbSNP Id: rs866424446

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224540_7224542del , CM000679.2:g.7224540_7224542del GRCh38
NC_000017.10:g.7127859_7127861del , CM000679.1:g.7127859_7127861del GRCh37
NC_000017.9:g.7068583_7068585del NCBI36
NG_007975.1:g.9707_9709del
NG_008391.2:g.512_514del
NG_033038.1:g.15006_15008del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1666_1668del MANE Select ENSP00000349297.5:p.Lys556del
ENST00000322910.9:c.*1621_*1623del ENSP00000325395.5:n.*1621_*1623del
ENST00000350303.9:c.1600_1602del ENSP00000344152.5:p.Lys534del
ENST00000356839.9:c.1666_1668del ENSP00000349297.5:p.Lys556del
ENST00000542255.6:c.524_526del
ENST00000543245.6:c.1735_1737del ENSP00000438689.2:p.Lys579del
ENST00000578319.5:n.247_249del
ENST00000578711.1:n.1036_1038del
ENST00000578809.5:n.238_240del
ENST00000579391.1:n.270_272del
ENST00000579425.5:n.782_784del
ENST00000579546.1:c.401_403del
ENST00000582450.1:n.174_176del
ENST00000583074.5:n.287_289del
ENST00000583848.5:c.52_54del ENSP00000466487.1:p.Lys18del
ENST00000583850.5:n.437_439del
ENST00000583858.5:c.597_599del
ENST00000585203.6:n.857_859del
NM_000018.3:c.1666_1668del NP_000009.1:p.Lys556del
NM_001033859.2:c.1600_1602del NP_001029031.1:p.Lys534del
NM_001270447.1:c.1735_1737del NP_001257376.1:p.Lys579del
NM_001270448.1:c.1438_1440del NP_001257377.1:p.Lys480del
XM_006721516.2:c.1666_1668del XP_006721579.2:p.Lys556del
XM_011523829.1:c.1564_1566del XP_011522131.1:p.Lys522del
XM_011523830.1:c.1564_1566del XP_011522132.1:p.Lys522del
XR_934021.1:n.1769_1771del
XR_934022.1:n.1675_1677del
XR_934023.1:n.1675_1677del
XM_006721516.3:c.1666_1668del XP_006721579.2:p.Lys556del
XM_011523829.2:c.1564_1566del XP_011522131.1:p.Lys522del
XM_011523830.2:c.1564_1566del XP_011522132.1:p.Lys522del
XM_024450741.1:c.1654_1656del XP_024306509.1:p.Lys552del
XR_934021.2:n.1721_1723del
XR_934022.2:n.1627_1629del
XR_934023.2:n.1627_1629del
NM_000018.4:c.1666_1668del MANE Select NP_000009.1:p.Lys556del
NM_001033859.3:c.1600_1602del NP_001029031.1:p.Lys534del
NM_001270447.2:c.1735_1737del NP_001257376.1:p.Lys579del
NM_001270448.2:c.1438_1440del NP_001257377.1:p.Lys480del