Canonical Allele Identifier: CA497694467

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7127700G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224381G>T , CM000679.2:g.7224381G>T	GRCh38
NC_000017.10:g.7127700G>T , CM000679.1:g.7127700G>T	GRCh37
NC_000017.9:g.7068424G>T	NCBI36
NG_007975.1:g.9548G>T
NG_008391.2:g.670C>A
NG_033038.1:g.15164C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1593G>T MANE Select	ENSP00000349297.5:p.Arg531=
ENST00000322910.9:c.*1548G>T	ENSP00000325395.5:n.*1548G>T
ENST00000350303.9:c.1527G>T	ENSP00000344152.5:p.Arg509=
ENST00000356839.9:c.1593G>T	ENSP00000349297.5:p.Arg531=
ENST00000542255.6:c.451G>T
ENST00000543245.6:c.1662G>T	ENSP00000438689.2:p.Arg554=
ENST00000578319.5:n.88G>T
ENST00000578711.1:n.877G>T
ENST00000578809.5:n.165G>T
ENST00000579391.1:n.201G>T
ENST00000579425.5:n.709G>T
ENST00000579546.1:c.332G>T
ENST00000579894.5:n.380G>T
ENST00000582450.1:n.101G>T
ENST00000583074.5:n.214G>T
ENST00000583850.5:n.368G>T
ENST00000583858.5:c.524G>T
ENST00000585203.6:n.784G>T
NM_000018.3:c.1593G>T	NP_000009.1:p.Arg531=
NM_001033859.2:c.1527G>T	NP_001029031.1:p.Arg509=
NM_001270447.1:c.1662G>T	NP_001257376.1:p.Arg554=
NM_001270448.1:c.1365G>T	NP_001257377.1:p.Arg455=
XM_006721516.2:c.1593G>T	XP_006721579.2:p.Arg531=
XM_011523829.1:c.1495G>T	XP_011522131.1:p.Glu499Ter
XM_011523830.1:c.1495G>T	XP_011522132.1:p.Glu499Ter
XR_934021.1:n.1700G>T
XR_934022.1:n.1602G>T
XR_934023.1:n.1602G>T
XM_006721516.3:c.1593G>T	XP_006721579.2:p.Arg531=
XM_011523829.2:c.1495G>T	XP_011522131.1:p.Glu499Ter
XM_011523830.2:c.1495G>T	XP_011522132.1:p.Glu499Ter
XM_024450741.1:c.1495G>T	XP_024306509.1:p.Glu499Ter
XR_934021.2:n.1652G>T
XR_934022.2:n.1554G>T
XR_934023.2:n.1554G>T
NM_000018.4:c.1593G>T MANE Select	NP_000009.1:p.Arg531=
NM_001033859.3:c.1527G>T	NP_001029031.1:p.Arg509=
NM_001270447.2:c.1662G>T	NP_001257376.1:p.Arg554=
NM_001270448.2:c.1365G>T	NP_001257377.1:p.Arg455=