Canonical Allele Identifier: CA497694250

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7128007C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224688C>G , CM000679.2:g.7224688C>G	GRCh38
NC_000017.10:g.7128007C>G , CM000679.1:g.7128007C>G	GRCh37
NC_000017.9:g.7068731C>G	NCBI36
NG_007975.1:g.9855C>G
NG_008391.2:g.363G>C
NG_033038.1:g.14857G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1725C>G MANE Select	ENSP00000349297.5:p.Leu575=
ENST00000322910.9:c.*1680C>G	ENSP00000325395.5:n.*1680C>G
ENST00000350303.9:c.1659C>G	ENSP00000344152.5:p.Leu553=
ENST00000356839.9:c.1725C>G	ENSP00000349297.5:p.Leu575=
ENST00000542255.6:c.537-27C>G
ENST00000543245.6:c.1794C>G	ENSP00000438689.2:p.Leu598=
ENST00000578033.1:n.56C>G
ENST00000578319.5:n.306C>G
ENST00000578711.1:n.1184C>G
ENST00000578809.5:n.297C>G
ENST00000579425.5:n.841C>G
ENST00000579546.1:c.460C>G
ENST00000583074.5:n.300-27C>G
ENST00000583848.5:c.91C>G	ENSP00000466487.1:p.Leu31Val
ENST00000583850.5:n.496C>G
ENST00000583858.5:c.656C>G
ENST00000585203.6:n.916C>G
NM_000018.3:c.1725C>G	NP_000009.1:p.Leu575=
NM_001033859.2:c.1659C>G	NP_001029031.1:p.Leu553=
NM_001270447.1:c.1794C>G	NP_001257376.1:p.Leu598=
NM_001270448.1:c.1497C>G	NP_001257377.1:p.Leu499=
XM_006721516.2:c.1679-27C>G	XP_006721579.2:n.1679-27C>G
XM_011523829.1:c.1577-27C>G	XP_011522131.1:n.1577-27C>G
XM_011523830.1:c.1623C>G	XP_011522132.1:p.Leu541=
XR_934021.1:n.1828C>G
XR_934022.1:n.1734C>G
XR_934023.1:n.1688-27C>G
XM_006721516.3:c.1679-27C>G	XP_006721579.2:n.1679-27C>G
XM_011523829.2:c.1577-27C>G	XP_011522131.1:n.1577-27C>G
XM_011523830.2:c.1623C>G	XP_011522132.1:p.Leu541=
XM_024450741.1:c.1713C>G	XP_024306509.1:p.Leu571=
XR_934021.2:n.1780C>G
XR_934022.2:n.1686C>G
XR_934023.2:n.1640-27C>G
NM_000018.4:c.1725C>G MANE Select	NP_000009.1:p.Leu575=
NM_001033859.3:c.1659C>G	NP_001029031.1:p.Leu553=
NM_001270447.2:c.1794C>G	NP_001257376.1:p.Leu598=
NM_001270448.2:c.1497C>G	NP_001257377.1:p.Leu499=