Canonical Allele Identifier: CA2245711901
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223815G= , CM000679.2:g.7223815G= GRCh38
NC_000017.10:g.7127134G= , CM000679.1:g.7127134G= GRCh37
NC_000017.9:g.7067858G= NCBI36
NG_007975.1:g.8982G=
NG_008391.2:g.1236C=
NG_033038.1:g.15730C=

Transcript Alleles

HGVS Amino-acid change
ENST00000356839.10:c.1272G= MANE Select ENSP00000349297.5:p.Glu424=
ENST00000322910.9:c.*1227G= ENSP00000325395.5:n.*1227G=
ENST00000350303.9:c.1206G= ENSP00000344152.5:p.Glu402=
ENST00000356839.9:c.1272G= ENSP00000349297.5:p.Glu424=
ENST00000542255.6:c.130G=
ENST00000543245.6:c.1341G= ENSP00000438689.2:p.Glu447=
ENST00000578579.2:n.443G=
ENST00000578711.1:n.311G=
ENST00000578824.5:n.688G=
ENST00000579425.5:n.296G=
ENST00000579546.1:c.109G=
ENST00000583850.5:n.47G=
ENST00000583858.5:c.301G=
ENST00000585203.6:n.480G=
NM_000018.3:c.1272G= NP_000009.1:p.Glu424=
NM_001033859.2:c.1206G= NP_001029031.1:p.Glu402=
NM_001270447.1:c.1341G= NP_001257376.1:p.Glu447=
NM_001270448.1:c.1044G= NP_001257377.1:p.Glu348=
XM_006721516.2:c.1272G= XP_006721579.2:p.Glu424=
XM_011523829.1:c.1272G= XP_011522131.1:p.Glu424=
XM_011523830.1:c.1272G= XP_011522132.1:p.Glu424=
XR_934021.1:n.1379G=
XR_934022.1:n.1379G=
XR_934023.1:n.1379G=
XM_006721516.3:c.1272G= XP_006721579.2:p.Glu424=
XM_011523829.2:c.1272G= XP_011522131.1:p.Glu424=
XM_011523830.2:c.1272G= XP_011522132.1:p.Glu424=
XM_024450741.1:c.1272G= XP_024306509.1:p.Glu424=
XR_934021.2:n.1331G=
XR_934022.2:n.1331G=
XR_934023.2:n.1331G=
NM_000018.4:c.1272G= MANE Select NP_000009.1:p.Glu424=
NM_001033859.3:c.1206G= NP_001029031.1:p.Glu402=
NM_001270447.2:c.1341G= NP_001257376.1:p.Glu447=
NM_001270448.2:c.1044G= NP_001257377.1:p.Glu348=