Canonical Allele Identifier: CA2245715486

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224778A= , CM000679.2:g.7224778A=	GRCh38
NC_000017.10:g.7128097A= , CM000679.1:g.7128097A=	GRCh37
NC_000017.9:g.7068821A=	NCBI36
NG_007975.1:g.9945A=
NG_008391.2:g.273T=
NG_033038.1:g.14767T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1752-31A= MANE Select	ENSP00000349297.5:n.1752-31A=
ENST00000322910.9:c.*1707-31A=	ENSP00000325395.5:n.*1707-31A=
ENST00000350303.9:c.1686-31A=	ENSP00000344152.5:n.1686-31A=
ENST00000356839.9:c.1752-31A=	ENSP00000349297.5:n.1752-31A=
ENST00000542255.6:c.600A=
ENST00000543245.6:c.1821-31A=	ENSP00000438689.2:n.1821-31A=
ENST00000578033.1:n.146A=
ENST00000578319.5:n.333-31A=
ENST00000578711.1:n.1274A=
ENST00000578809.5:n.324-31A=
ENST00000579425.5:n.868-31A=
ENST00000579546.1:c.487-31A=
ENST00000583074.5:n.363A=
ENST00000583848.5:c.118-31A=	ENSP00000466487.1:n.118-31A=
ENST00000583850.5:n.523-31A=
ENST00000583858.5:c.683-31A=
ENST00000585203.6:n.943-31A=
NM_000018.3:c.1752-31A=	NP_000009.1:n.1752-31A=
NM_001033859.2:c.1686-31A=	NP_001029031.1:n.1686-31A=
NM_001270447.1:c.1821-31A=	NP_001257376.1:n.1821-31A=
NM_001270448.1:c.1524-31A=	NP_001257377.1:n.1524-31A=
XM_006721516.2:c.1742A=	XP_006721579.2:p.Gln581=
XM_011523829.1:c.1640A=	XP_011522131.1:p.Gln547=
XM_011523830.1:c.1650-31A=	XP_011522132.1:n.1650-31A=
XR_934021.1:n.1855-31A=
XR_934022.1:n.1761-31A=
XR_934023.1:n.1751A=
XM_006721516.3:c.1742A=	XP_006721579.2:p.Gln581=
XM_011523829.2:c.1640A=	XP_011522131.1:p.Gln547=
XM_011523830.2:c.1650-31A=	XP_011522132.1:n.1650-31A=
XM_024450741.1:c.1740-31A=	XP_024306509.1:n.1740-31A=
XR_934021.2:n.1807-31A=
XR_934022.2:n.1713-31A=
XR_934023.2:n.1703A=
NM_000018.4:c.1752-31A= MANE Select	NP_000009.1:n.1752-31A=
NM_001033859.3:c.1686-31A=	NP_001029031.1:n.1686-31A=
NM_001270447.2:c.1821-31A=	NP_001257376.1:n.1821-31A=
NM_001270448.2:c.1524-31A=	NP_001257377.1:n.1524-31A=