Canonical Allele Identifier: CA2245716675

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7225107G= , CM000679.2:g.7225107G=	GRCh38
NC_000017.10:g.7128426G= , CM000679.1:g.7128426G=	GRCh37
NC_000017.9:g.7069150G=	NCBI36
NG_007975.1:g.10274G=
NG_033038.1:g.14438C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.*10G= MANE Select	ENSP00000349297.5:n.*10G=
ENST00000322910.9:c.*1933G=	ENSP00000325395.5:n.*1933G=
ENST00000350303.9:c.*10G=	ENSP00000344152.5:n.*10G=
ENST00000356839.9:c.*10G=	ENSP00000349297.5:n.*10G=
ENST00000542255.6:c.857G=
ENST00000543245.6:c.*10G=	ENSP00000438689.2:n.*10G=
ENST00000578033.1:n.403G=
ENST00000578319.5:n.559G=
ENST00000578711.1:n.1603G=
ENST00000578809.5:n.550G=
ENST00000579425.5:n.1094G=
ENST00000583848.5:c.344G=	ENSP00000466487.1:n.344G=
ENST00000583850.5:n.749G=
ENST00000583858.5:c.909G=
NM_000018.3:c.*10G=	NP_000009.1:n.*10G=
NM_001033859.2:c.*10G=	NP_001029031.1:n.*10G=
NM_001270447.1:c.*10G=	NP_001257376.1:n.*10G=
NM_001270448.1:c.*10G=	NP_001257377.1:n.*10G=
XM_006721516.2:c.*10G=	XP_006721579.2:n.*10G=
XM_011523829.1:c.*10G=	XP_011522131.1:n.*10G=
XM_011523830.1:c.*10G=	XP_011522132.1:n.*10G=
XR_934021.1:n.2081G=
XR_934022.1:n.1987G=
XR_934023.1:n.2008G=
XM_006721516.3:c.*10G=	XP_006721579.2:n.*10G=
XM_011523829.2:c.*10G=	XP_011522131.1:n.*10G=
XM_011523830.2:c.*10G=	XP_011522132.1:n.*10G=
XM_024450741.1:c.*10G=	XP_024306509.1:n.*10G=
XR_934021.2:n.2033G=
XR_934022.2:n.1939G=
XR_934023.2:n.1960G=
NM_000018.4:c.*10G= MANE Select	NP_000009.1:n.*10G=
NM_001033859.3:c.*10G=	NP_001029031.1:n.*10G=
NM_001270447.2:c.*10G=	NP_001257376.1:n.*10G=
NM_001270448.2:c.*10G=	NP_001257377.1:n.*10G=