Canonical Allele Identifier: CA2245712758
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224039T= , CM000679.2:g.7224039T= GRCh38
NC_000017.10:g.7127358T= , CM000679.1:g.7127358T= GRCh37
NC_000017.9:g.7068082T= NCBI36
NG_007975.1:g.9206T=
NG_008391.2:g.1012A=
NG_033038.1:g.15506A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1404T= MANE Select ENSP00000349297.5:p.Leu468=
ENST00000322910.9:c.*1359T= ENSP00000325395.5:n.*1359T=
ENST00000350303.9:c.1338T= ENSP00000344152.5:p.Leu446=
ENST00000356839.9:c.1404T= ENSP00000349297.5:p.Leu468=
ENST00000542255.6:c.262T=
ENST00000543245.6:c.1473T= ENSP00000438689.2:p.Leu491=
ENST00000578711.1:n.535T=
ENST00000579425.5:n.520T=
ENST00000579546.1:c.241T=
ENST00000579894.5:n.115T=
ENST00000583074.5:n.123T=
ENST00000583850.5:n.179T=
ENST00000583858.5:c.433T=
ENST00000585203.6:n.595T=
NM_000018.3:c.1404T= NP_000009.1:p.Leu468=
NM_001033859.2:c.1338T= NP_001029031.1:p.Leu446=
NM_001270447.1:c.1473T= NP_001257376.1:p.Leu491=
NM_001270448.1:c.1176T= NP_001257377.1:p.Leu392=
XM_006721516.2:c.1404T= XP_006721579.2:p.Leu468=
XM_011523829.1:c.1404T= XP_011522131.1:p.Leu468=
XM_011523830.1:c.1404T= XP_011522132.1:p.Leu468=
XR_934021.1:n.1511T=
XR_934022.1:n.1511T=
XR_934023.1:n.1511T=
XM_006721516.3:c.1404T= XP_006721579.2:p.Leu468=
XM_011523829.2:c.1404T= XP_011522131.1:p.Leu468=
XM_011523830.2:c.1404T= XP_011522132.1:p.Leu468=
XM_024450741.1:c.1404T= XP_024306509.1:p.Leu468=
XR_934021.2:n.1463T=
XR_934022.2:n.1463T=
XR_934023.2:n.1463T=
NM_000018.4:c.1404T= MANE Select NP_000009.1:p.Leu468=
NM_001033859.3:c.1338T= NP_001029031.1:p.Leu446=
NM_001270447.2:c.1473T= NP_001257376.1:p.Leu491=
NM_001270448.2:c.1176T= NP_001257377.1:p.Leu392=