Canonical Allele Identifier: CA397726105

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7128334A>G (hg19) ; chr17:g.7225015A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7225015A>G , CM000679.2:g.7225015A>G	GRCh38
NC_000017.10:g.7128334A>G , CM000679.1:g.7128334A>G	GRCh37
NC_000017.9:g.7069058A>G	NCBI36
NG_007975.1:g.10182A>G
NG_008391.2:g.36T>C
NG_033038.1:g.14530T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1886A>G MANE Select	ENSP00000349297.5:p.Glu629Gly
ENST00000322910.9:c.*1841A>G	ENSP00000325395.5:n.*1841A>G
ENST00000350303.9:c.1820A>G	ENSP00000344152.5:p.Glu607Gly
ENST00000356839.9:c.1886A>G	ENSP00000349297.5:p.Glu629Gly
ENST00000542255.6:c.765A>G
ENST00000543245.6:c.1955A>G	ENSP00000438689.2:p.Glu652Gly
ENST00000578033.1:n.311A>G
ENST00000578319.5:n.467A>G
ENST00000578711.1:n.1511A>G
ENST00000578809.5:n.458A>G
ENST00000579425.5:n.1002A>G
ENST00000583848.5:c.252A>G	ENSP00000466487.1:n.252A>G
ENST00000583850.5:n.657A>G
ENST00000583858.5:c.817A>G
NM_000018.3:c.1886A>G	NP_000009.1:p.Glu629Gly
NM_001033859.2:c.1820A>G	NP_001029031.1:p.Glu607Gly
NM_001270447.1:c.1955A>G	NP_001257376.1:p.Glu652Gly
NM_001270448.1:c.1658A>G	NP_001257377.1:p.Glu553Gly
XM_006721516.2:c.1907A>G	XP_006721579.2:p.Glu636Gly
XM_011523829.1:c.1805A>G	XP_011522131.1:p.Glu602Gly
XM_011523830.1:c.1784A>G	XP_011522132.1:p.Glu595Gly
XR_934021.1:n.1989A>G
XR_934022.1:n.1895A>G
XR_934023.1:n.1916A>G
XM_006721516.3:c.1907A>G	XP_006721579.2:p.Glu636Gly
XM_011523829.2:c.1805A>G	XP_011522131.1:p.Glu602Gly
XM_011523830.2:c.1784A>G	XP_011522132.1:p.Glu595Gly
XM_024450741.1:c.1874A>G	XP_024306509.1:p.Glu625Gly
XR_934021.2:n.1941A>G
XR_934022.2:n.1847A>G
XR_934023.2:n.1868A>G
NM_000018.4:c.1886A>G MANE Select	NP_000009.1:p.Glu629Gly
NM_001033859.3:c.1820A>G	NP_001029031.1:p.Glu607Gly
NM_001270447.2:c.1955A>G	NP_001257376.1:p.Glu652Gly
NM_001270448.2:c.1658A>G	NP_001257377.1:p.Glu553Gly