Canonical Allele Identifier: CA2245715529
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224791T= , CM000679.2:g.7224791T= GRCh38
NC_000017.10:g.7128110T= , CM000679.1:g.7128110T= GRCh37
NC_000017.9:g.7068834T= NCBI36
NG_007975.1:g.9958T=
NG_008391.2:g.260A=
NG_033038.1:g.14754A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1752-18T= MANE Select ENSP00000349297.5:n.1752-18T=
ENST00000322910.9:c.*1707-18T= ENSP00000325395.5:n.*1707-18T=
ENST00000350303.9:c.1686-18T= ENSP00000344152.5:n.1686-18T=
ENST00000356839.9:c.1752-18T= ENSP00000349297.5:n.1752-18T=
ENST00000542255.6:c.613T=
ENST00000543245.6:c.1821-18T= ENSP00000438689.2:n.1821-18T=
ENST00000578033.1:n.159T=
ENST00000578319.5:n.333-18T=
ENST00000578711.1:n.1287T=
ENST00000578809.5:n.324-18T=
ENST00000579425.5:n.868-18T=
ENST00000579546.1:c.487-18T=
ENST00000583074.5:n.376T=
ENST00000583848.5:c.118-18T= ENSP00000466487.1:n.118-18T=
ENST00000583850.5:n.523-18T=
ENST00000583858.5:c.683-18T=
ENST00000585203.6:n.943-18T=
NM_000018.3:c.1752-18T= NP_000009.1:n.1752-18T=
NM_001033859.2:c.1686-18T= NP_001029031.1:n.1686-18T=
NM_001270447.1:c.1821-18T= NP_001257376.1:n.1821-18T=
NM_001270448.1:c.1524-18T= NP_001257377.1:n.1524-18T=
XM_006721516.2:c.1755T= XP_006721579.2:p.His585=
XM_011523829.1:c.1653T= XP_011522131.1:p.His551=
XM_011523830.1:c.1650-18T= XP_011522132.1:n.1650-18T=
XR_934021.1:n.1855-18T=
XR_934022.1:n.1761-18T=
XR_934023.1:n.1764T=
XM_006721516.3:c.1755T= XP_006721579.2:p.His585=
XM_011523829.2:c.1653T= XP_011522131.1:p.His551=
XM_011523830.2:c.1650-18T= XP_011522132.1:n.1650-18T=
XM_024450741.1:c.1740-18T= XP_024306509.1:n.1740-18T=
XR_934021.2:n.1807-18T=
XR_934022.2:n.1713-18T=
XR_934023.2:n.1716T=
NM_000018.4:c.1752-18T= MANE Select NP_000009.1:n.1752-18T=
NM_001033859.3:c.1686-18T= NP_001029031.1:n.1686-18T=
NM_001270447.2:c.1821-18T= NP_001257376.1:n.1821-18T=
NM_001270448.2:c.1524-18T= NP_001257377.1:n.1524-18T=