Canonical Allele Identifier: CA497694376
Gene: ACADVL HGNC NCBI

Linked Data

ClinVar Variation Id: 1569750
ClinVar RCV Id: RCV002220913
dbSNP Id: rs2142987170
gnomAD v4: 17-7224241-G-A
MyVariant Identifiers: chr17:g.7127560G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224241G>A , CM000679.2:g.7224241G>A GRCh38
NC_000017.10:g.7127560G>A , CM000679.1:g.7127560G>A GRCh37
NC_000017.9:g.7068284G>A NCBI36
NG_007975.1:g.9408G>A
NG_008391.2:g.810C>T
NG_033038.1:g.15304C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1530G>A MANE Select ENSP00000349297.5:p.Arg510=
ENST00000322910.9:c.*1485G>A ENSP00000325395.5:n.*1485G>A
ENST00000350303.9:c.1464G>A ENSP00000344152.5:p.Arg488=
ENST00000356839.9:c.1530G>A ENSP00000349297.5:p.Arg510=
ENST00000542255.6:c.388G>A
ENST00000543245.6:c.1599G>A ENSP00000438689.2:p.Arg533=
ENST00000578319.5:n.25G>A
ENST00000578711.1:n.737G>A
ENST00000578809.5:n.25G>A
ENST00000579391.1:n.138G>A
ENST00000579425.5:n.646G>A
ENST00000579546.1:c.272-80G>A
ENST00000579894.5:n.317G>A
ENST00000583074.5:n.154-80G>A
ENST00000583850.5:n.305G>A
ENST00000583858.5:c.464-80G>A
ENST00000585203.6:n.721G>A
NM_000018.3:c.1530G>A NP_000009.1:p.Arg510=
NM_001033859.2:c.1464G>A NP_001029031.1:p.Arg488=
NM_001270447.1:c.1599G>A NP_001257376.1:p.Arg533=
NM_001270448.1:c.1302G>A NP_001257377.1:p.Arg434=
XM_006721516.2:c.1530G>A XP_006721579.2:p.Arg510=
XM_011523829.1:c.1435-80G>A XP_011522131.1:n.1435-80G>A
XM_011523830.1:c.1435-80G>A XP_011522132.1:n.1435-80G>A
XR_934021.1:n.1637G>A
XR_934022.1:n.1542-80G>A
XR_934023.1:n.1542-80G>A
XM_006721516.3:c.1530G>A XP_006721579.2:p.Arg510=
XM_011523829.2:c.1435-80G>A XP_011522131.1:n.1435-80G>A
XM_011523830.2:c.1435-80G>A XP_011522132.1:n.1435-80G>A
XM_024450741.1:c.1435-80G>A XP_024306509.1:n.1435-80G>A
XR_934021.2:n.1589G>A
XR_934022.2:n.1494-80G>A
XR_934023.2:n.1494-80G>A
NM_000018.4:c.1530G>A MANE Select NP_000009.1:p.Arg510=
NM_001033859.3:c.1464G>A NP_001029031.1:p.Arg488=
NM_001270447.2:c.1599G>A NP_001257376.1:p.Arg533=
NM_001270448.2:c.1302G>A NP_001257377.1:p.Arg434=