Canonical Allele Identifier: CA2245712769

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224043C= , CM000679.2:g.7224043C=	GRCh38
NC_000017.10:g.7127362C= , CM000679.1:g.7127362C=	GRCh37
NC_000017.9:g.7068086C=	NCBI36
NG_007975.1:g.9210C=
NG_008391.2:g.1008G=
NG_033038.1:g.15502G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1408C= MANE Select	ENSP00000349297.5:p.Leu470=
ENST00000322910.9:c.*1363C=	ENSP00000325395.5:n.*1363C=
ENST00000350303.9:c.1342C=	ENSP00000344152.5:p.Leu448=
ENST00000356839.9:c.1408C=	ENSP00000349297.5:p.Leu470=
ENST00000542255.6:c.266C=
ENST00000543245.6:c.1477C=	ENSP00000438689.2:p.Leu493=
ENST00000578711.1:n.539C=
ENST00000579425.5:n.524C=
ENST00000579546.1:c.245C=
ENST00000579894.5:n.119C=
ENST00000583074.5:n.127C=
ENST00000583850.5:n.183C=
ENST00000583858.5:c.437C=
ENST00000585203.6:n.599C=
NM_000018.3:c.1408C=	NP_000009.1:p.Leu470=
NM_001033859.2:c.1342C=	NP_001029031.1:p.Leu448=
NM_001270447.1:c.1477C=	NP_001257376.1:p.Leu493=
NM_001270448.1:c.1180C=	NP_001257377.1:p.Leu394=
XM_006721516.2:c.1408C=	XP_006721579.2:p.Leu470=
XM_011523829.1:c.1408C=	XP_011522131.1:p.Leu470=
XM_011523830.1:c.1408C=	XP_011522132.1:p.Leu470=
XR_934021.1:n.1515C=
XR_934022.1:n.1515C=
XR_934023.1:n.1515C=
XM_006721516.3:c.1408C=	XP_006721579.2:p.Leu470=
XM_011523829.2:c.1408C=	XP_011522131.1:p.Leu470=
XM_011523830.2:c.1408C=	XP_011522132.1:p.Leu470=
XM_024450741.1:c.1408C=	XP_024306509.1:p.Leu470=
XR_934021.2:n.1467C=
XR_934022.2:n.1467C=
XR_934023.2:n.1467C=
NM_000018.4:c.1408C= MANE Select	NP_000009.1:p.Leu470=
NM_001033859.3:c.1342C=	NP_001029031.1:p.Leu448=
NM_001270447.2:c.1477C=	NP_001257376.1:p.Leu493=
NM_001270448.2:c.1180C=	NP_001257377.1:p.Leu394=