Canonical Allele Identifier: CA2245716694

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7225123G= , CM000679.2:g.7225123G=	GRCh38
NC_000017.10:g.7128442G= , CM000679.1:g.7128442G=	GRCh37
NC_000017.9:g.7069166G=	NCBI36
NG_007975.1:g.10290G=
NG_033038.1:g.14422C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.*26G= MANE Select	ENSP00000349297.5:n.*26G=
ENST00000322910.9:c.*1949G=	ENSP00000325395.5:n.*1949G=
ENST00000350303.9:c.*26G=	ENSP00000344152.5:n.*26G=
ENST00000356839.9:c.*26G=	ENSP00000349297.5:n.*26G=
ENST00000542255.6:c.873G=
ENST00000543245.6:c.*26G=	ENSP00000438689.2:n.*26G=
ENST00000578033.1:n.419G=
ENST00000578319.5:n.575G=
ENST00000578711.1:n.1619G=
ENST00000578809.5:n.566G=
ENST00000579425.5:n.1110G=
ENST00000583848.5:c.360G=	ENSP00000466487.1:n.360G=
ENST00000583850.5:n.765G=
ENST00000583858.5:c.925G=
NM_000018.3:c.*26G=	NP_000009.1:n.*26G=
NM_001033859.2:c.*26G=	NP_001029031.1:n.*26G=
NM_001270447.1:c.*26G=	NP_001257376.1:n.*26G=
NM_001270448.1:c.*26G=	NP_001257377.1:n.*26G=
XM_006721516.2:c.*26G=	XP_006721579.2:n.*26G=
XM_011523829.1:c.*26G=	XP_011522131.1:n.*26G=
XM_011523830.1:c.*26G=	XP_011522132.1:n.*26G=
XR_934021.1:n.2097G=
XR_934022.1:n.2003G=
XR_934023.1:n.2024G=
XM_006721516.3:c.*26G=	XP_006721579.2:n.*26G=
XM_011523829.2:c.*26G=	XP_011522131.1:n.*26G=
XM_011523830.2:c.*26G=	XP_011522132.1:n.*26G=
XM_024450741.1:c.*26G=	XP_024306509.1:n.*26G=
XR_934021.2:n.2049G=
XR_934022.2:n.1955G=
XR_934023.2:n.1976G=
NM_000018.4:c.*26G= MANE Select	NP_000009.1:n.*26G=
NM_001033859.3:c.*26G=	NP_001029031.1:n.*26G=
NM_001270447.2:c.*26G=	NP_001257376.1:n.*26G=
NM_001270448.2:c.*26G=	NP_001257377.1:n.*26G=