Canonical Allele Identifier: CA397725657
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224648A>T , CM000679.2:g.7224648A>T GRCh38
NC_000017.10:g.7127967A>T , CM000679.1:g.7127967A>T GRCh37
NC_000017.9:g.7068691A>T NCBI36
NG_007975.1:g.9815A>T
NG_008391.2:g.403T>A
NG_033038.1:g.14897T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000356839.10:c.1685A>T MANE Select ENSP00000349297.5:p.Gln562Leu
ENST00000322910.9:c.*1640A>T ENSP00000325395.5:n.*1640A>T
ENST00000350303.9:c.1619A>T ENSP00000344152.5:p.Gln540Leu
ENST00000356839.9:c.1685A>T ENSP00000349297.5:p.Gln562Leu
ENST00000542255.6:c.537-67A>T
ENST00000543245.6:c.1754A>T ENSP00000438689.2:p.Gln585Leu
ENST00000578033.1:n.16A>T
ENST00000578319.5:n.266A>T
ENST00000578711.1:n.1144A>T
ENST00000578809.5:n.257A>T
ENST00000579425.5:n.801A>T
ENST00000579546.1:c.420A>T
ENST00000582450.1:n.282A>T
ENST00000583074.5:n.300-67A>T
ENST00000583848.5:c.65-14A>T ENSP00000466487.1:n.65-14A>T
ENST00000583850.5:n.456A>T
ENST00000583858.5:c.616A>T
ENST00000585203.6:n.876A>T
NM_000018.3:c.1685A>T NP_000009.1:p.Gln562Leu
NM_001033859.2:c.1619A>T NP_001029031.1:p.Gln540Leu
NM_001270447.1:c.1754A>T NP_001257376.1:p.Gln585Leu
NM_001270448.1:c.1457A>T NP_001257377.1:p.Gln486Leu
XM_006721516.2:c.1679-67A>T XP_006721579.2:n.1679-67A>T
XM_011523829.1:c.1577-67A>T XP_011522131.1:n.1577-67A>T
XM_011523830.1:c.1583A>T XP_011522132.1:p.Gln528Leu
XR_934021.1:n.1788A>T
XR_934022.1:n.1694A>T
XR_934023.1:n.1688-67A>T
XM_006721516.3:c.1679-67A>T XP_006721579.2:n.1679-67A>T
XM_011523829.2:c.1577-67A>T XP_011522131.1:n.1577-67A>T
XM_011523830.2:c.1583A>T XP_011522132.1:p.Gln528Leu
XM_024450741.1:c.1673A>T XP_024306509.1:p.Gln558Leu
XR_934021.2:n.1740A>T
XR_934022.2:n.1646A>T
XR_934023.2:n.1640-67A>T
NM_000018.4:c.1685A>T MANE Select NP_000009.1:p.Gln562Leu
NM_001033859.3:c.1619A>T NP_001029031.1:p.Gln540Leu
NM_001270447.2:c.1754A>T NP_001257376.1:p.Gln585Leu
NM_001270448.2:c.1457A>T NP_001257377.1:p.Gln486Leu