Canonical Allele Identifier: CA397725782

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7128027T>A (hg19) ; chr17:g.7224708T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224708T>A , CM000679.2:g.7224708T>A	GRCh38
NC_000017.10:g.7128027T>A , CM000679.1:g.7128027T>A	GRCh37
NC_000017.9:g.7068751T>A	NCBI36
NG_007975.1:g.9875T>A
NG_008391.2:g.343A>T
NG_033038.1:g.14837A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1745T>A MANE Select	ENSP00000349297.5:p.Leu582His
ENST00000322910.9:c.*1700T>A	ENSP00000325395.5:n.*1700T>A
ENST00000350303.9:c.1679T>A	ENSP00000344152.5:p.Leu560His
ENST00000356839.9:c.1745T>A	ENSP00000349297.5:p.Leu582His
ENST00000542255.6:c.537-7T>A
ENST00000543245.6:c.1814T>A	ENSP00000438689.2:p.Leu605His
ENST00000578033.1:n.76T>A
ENST00000578319.5:n.326T>A
ENST00000578711.1:n.1204T>A
ENST00000578809.5:n.317T>A
ENST00000579425.5:n.861T>A
ENST00000579546.1:c.480T>A
ENST00000583074.5:n.300-7T>A
ENST00000583848.5:c.111T>A	ENSP00000466487.1:p.Ser37=
ENST00000583850.5:n.516T>A
ENST00000583858.5:c.676T>A
ENST00000585203.6:n.936T>A
NM_000018.3:c.1745T>A	NP_000009.1:p.Leu582His
NM_001033859.2:c.1679T>A	NP_001029031.1:p.Leu560His
NM_001270447.1:c.1814T>A	NP_001257376.1:p.Leu605His
NM_001270448.1:c.1517T>A	NP_001257377.1:p.Leu506His
XM_006721516.2:c.1679-7T>A	XP_006721579.2:n.1679-7T>A
XM_011523829.1:c.1577-7T>A	XP_011522131.1:n.1577-7T>A
XM_011523830.1:c.1643T>A	XP_011522132.1:p.Leu548His
XR_934021.1:n.1848T>A
XR_934022.1:n.1754T>A
XR_934023.1:n.1688-7T>A
XM_006721516.3:c.1679-7T>A	XP_006721579.2:n.1679-7T>A
XM_011523829.2:c.1577-7T>A	XP_011522131.1:n.1577-7T>A
XM_011523830.2:c.1643T>A	XP_011522132.1:p.Leu548His
XM_024450741.1:c.1733T>A	XP_024306509.1:p.Leu578His
XR_934021.2:n.1800T>A
XR_934022.2:n.1706T>A
XR_934023.2:n.1640-7T>A
NM_000018.4:c.1745T>A MANE Select	NP_000009.1:p.Leu582His
NM_001033859.3:c.1679T>A	NP_001029031.1:p.Leu560His
NM_001270447.2:c.1814T>A	NP_001257376.1:p.Leu605His
NM_001270448.2:c.1517T>A	NP_001257377.1:p.Leu506His