Canonical Allele Identifier: CA8337863
Gene: ACADVL HGNC NCBI

Linked Data

ClinVar Variation Id: 1517801
ClinVar RCV Id: RCV002027618
dbSNP Id: rs1208459885
gnomAD v2: 17-7125572-G-A
gnomAD v4: 17-7222253-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222253G>A , CM000679.2:g.7222253G>A GRCh38
NC_000017.10:g.7125572G>A , CM000679.1:g.7125572G>A GRCh37
NC_000017.9:g.7066296G>A NCBI36
NG_007975.1:g.7420G>A
NG_008391.2:g.2798C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.829G>A MANE Select ENSP00000349297.5:p.Glu277Lys
ENST00000322910.9:c.*784G>A ENSP00000325395.5:n.*784G>A
ENST00000350303.9:c.763G>A ENSP00000344152.5:p.Glu255Lys
ENST00000356839.9:c.829G>A ENSP00000349297.5:p.Glu277Lys
ENST00000543245.6:c.898G>A ENSP00000438689.2:p.Glu300Lys
ENST00000577191.5:n.1001G>A
ENST00000581378.5:c.547G>A
ENST00000582379.1:n.213G>A
NM_000018.3:c.829G>A NP_000009.1:p.Glu277Lys
NM_001033859.2:c.763G>A NP_001029031.1:p.Glu255Lys
NM_001270447.1:c.898G>A NP_001257376.1:p.Glu300Lys
NM_001270448.1:c.601G>A NP_001257377.1:p.Glu201Lys
XM_006721516.2:c.829G>A XP_006721579.2:p.Glu277Lys
XM_011523829.1:c.829G>A XP_011522131.1:p.Glu277Lys
XM_011523830.1:c.829G>A XP_011522132.1:p.Glu277Lys
XR_934021.1:n.936G>A
XR_934022.1:n.936G>A
XR_934023.1:n.936G>A
XM_006721516.3:c.829G>A XP_006721579.2:p.Glu277Lys
XM_011523829.2:c.829G>A XP_011522131.1:p.Glu277Lys
XM_011523830.2:c.829G>A XP_011522132.1:p.Glu277Lys
XM_024450741.1:c.829G>A XP_024306509.1:p.Glu277Lys
XR_934021.2:n.888G>A
XR_934022.2:n.888G>A
XR_934023.2:n.888G>A
NM_000018.4:c.829G>A MANE Select NP_000009.1:p.Glu277Lys
NM_001033859.3:c.763G>A NP_001029031.1:p.Glu255Lys
NM_001270447.2:c.898G>A NP_001257376.1:p.Glu300Lys
NM_001270448.2:c.601G>A NP_001257377.1:p.Glu201Lys