Canonical Allele Identifier: CA2245715415

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224767C= , CM000679.2:g.7224767C=	GRCh38
NC_000017.10:g.7128086C= , CM000679.1:g.7128086C=	GRCh37
NC_000017.9:g.7068810C=	NCBI36
NG_007975.1:g.9934C=
NG_008391.2:g.284G=
NG_033038.1:g.14778G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1752-42C= MANE Select	ENSP00000349297.5:n.1752-42C=
ENST00000322910.9:c.*1707-42C=	ENSP00000325395.5:n.*1707-42C=
ENST00000350303.9:c.1686-42C=	ENSP00000344152.5:n.1686-42C=
ENST00000356839.9:c.1752-42C=	ENSP00000349297.5:n.1752-42C=
ENST00000542255.6:c.589C=
ENST00000543245.6:c.1821-42C=	ENSP00000438689.2:n.1821-42C=
ENST00000578033.1:n.135C=
ENST00000578319.5:n.333-42C=
ENST00000578711.1:n.1263C=
ENST00000578809.5:n.324-42C=
ENST00000579425.5:n.868-42C=
ENST00000579546.1:c.487-42C=
ENST00000583074.5:n.352C=
ENST00000583848.5:c.118-42C=	ENSP00000466487.1:n.118-42C=
ENST00000583850.5:n.523-42C=
ENST00000583858.5:c.683-42C=
ENST00000585203.6:n.943-42C=
NM_000018.3:c.1752-42C=	NP_000009.1:n.1752-42C=
NM_001033859.2:c.1686-42C=	NP_001029031.1:n.1686-42C=
NM_001270447.1:c.1821-42C=	NP_001257376.1:n.1821-42C=
NM_001270448.1:c.1524-42C=	NP_001257377.1:n.1524-42C=
XM_006721516.2:c.1731C=	XP_006721579.2:p.Ser577=
XM_011523829.1:c.1629C=	XP_011522131.1:p.Ser543=
XM_011523830.1:c.1650-42C=	XP_011522132.1:n.1650-42C=
XR_934021.1:n.1855-42C=
XR_934022.1:n.1761-42C=
XR_934023.1:n.1740C=
XM_006721516.3:c.1731C=	XP_006721579.2:p.Ser577=
XM_011523829.2:c.1629C=	XP_011522131.1:p.Ser543=
XM_011523830.2:c.1650-42C=	XP_011522132.1:n.1650-42C=
XM_024450741.1:c.1740-42C=	XP_024306509.1:n.1740-42C=
XR_934021.2:n.1807-42C=
XR_934022.2:n.1713-42C=
XR_934023.2:n.1692C=
NM_000018.4:c.1752-42C= MANE Select	NP_000009.1:n.1752-42C=
NM_001033859.3:c.1686-42C=	NP_001029031.1:n.1686-42C=
NM_001270447.2:c.1821-42C=	NP_001257376.1:n.1821-42C=
NM_001270448.2:c.1524-42C=	NP_001257377.1:n.1524-42C=