Canonical Allele Identifier: CA397726200

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7128376A>T (hg19) ; chr17:g.7225057A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7225057A>T , CM000679.2:g.7225057A>T	GRCh38
NC_000017.10:g.7128376A>T , CM000679.1:g.7128376A>T	GRCh37
NC_000017.9:g.7069100A>T	NCBI36
NG_007975.1:g.10224A>T
NG_033038.1:g.14488T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1928A>T MANE Select	ENSP00000349297.5:p.Glu643Val
ENST00000322910.9:c.*1883A>T	ENSP00000325395.5:n.*1883A>T
ENST00000350303.9:c.1862A>T	ENSP00000344152.5:p.Glu621Val
ENST00000356839.9:c.1928A>T	ENSP00000349297.5:p.Glu643Val
ENST00000542255.6:c.807A>T
ENST00000543245.6:c.1997A>T	ENSP00000438689.2:p.Glu666Val
ENST00000578033.1:n.353A>T
ENST00000578319.5:n.509A>T
ENST00000578711.1:n.1553A>T
ENST00000578809.5:n.500A>T
ENST00000579425.5:n.1044A>T
ENST00000583848.5:c.294A>T	ENSP00000466487.1:n.294A>T
ENST00000583850.5:n.699A>T
ENST00000583858.5:c.859A>T
NM_000018.3:c.1928A>T	NP_000009.1:p.Glu643Val
NM_001033859.2:c.1862A>T	NP_001029031.1:p.Glu621Val
NM_001270447.1:c.1997A>T	NP_001257376.1:p.Glu666Val
NM_001270448.1:c.1700A>T	NP_001257377.1:p.Glu567Val
XM_006721516.2:c.1949A>T	XP_006721579.2:p.Glu650Val
XM_011523829.1:c.1847A>T	XP_011522131.1:p.Glu616Val
XM_011523830.1:c.1826A>T	XP_011522132.1:p.Glu609Val
XR_934021.1:n.2031A>T
XR_934022.1:n.1937A>T
XR_934023.1:n.1958A>T
XM_006721516.3:c.1949A>T	XP_006721579.2:p.Glu650Val
XM_011523829.2:c.1847A>T	XP_011522131.1:p.Glu616Val
XM_011523830.2:c.1826A>T	XP_011522132.1:p.Glu609Val
XM_024450741.1:c.1916A>T	XP_024306509.1:p.Glu639Val
XR_934021.2:n.1983A>T
XR_934022.2:n.1889A>T
XR_934023.2:n.1910A>T
NM_000018.4:c.1928A>T MANE Select	NP_000009.1:p.Glu643Val
NM_001033859.3:c.1862A>T	NP_001029031.1:p.Glu621Val
NM_001270447.2:c.1997A>T	NP_001257376.1:p.Glu666Val
NM_001270448.2:c.1700A>T	NP_001257377.1:p.Glu567Val