Canonical Allele Identifier: CA397725295
Gene: ACADVL HGNC NCBI

Linked Data

ClinVar Variation Id: 2035405
ClinVar RCV Id: RCV002877497

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224231A>T , CM000679.2:g.7224231A>T GRCh38
NC_000017.10:g.7127550A>T , CM000679.1:g.7127550A>T GRCh37
NC_000017.9:g.7068274A>T NCBI36
NG_007975.1:g.9398A>T
NG_008391.2:g.820T>A
NG_033038.1:g.15314T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1520A>T MANE Select ENSP00000349297.5:p.Lys507Ile
ENST00000322910.9:c.*1475A>T ENSP00000325395.5:n.*1475A>T
ENST00000350303.9:c.1454A>T ENSP00000344152.5:p.Lys485Ile
ENST00000356839.9:c.1520A>T ENSP00000349297.5:p.Lys507Ile
ENST00000542255.6:c.378A>T
ENST00000543245.6:c.1589A>T ENSP00000438689.2:p.Lys530Ile
ENST00000578319.5:n.15A>T
ENST00000578711.1:n.727A>T
ENST00000578809.5:n.15A>T
ENST00000579391.1:n.128A>T
ENST00000579425.5:n.636A>T
ENST00000579546.1:c.272-90A>T
ENST00000579894.5:n.307A>T
ENST00000583074.5:n.154-90A>T
ENST00000583850.5:n.295A>T
ENST00000583858.5:c.464-90A>T
ENST00000585203.6:n.711A>T
NM_000018.3:c.1520A>T NP_000009.1:p.Lys507Ile
NM_001033859.2:c.1454A>T NP_001029031.1:p.Lys485Ile
NM_001270447.1:c.1589A>T NP_001257376.1:p.Lys530Ile
NM_001270448.1:c.1292A>T NP_001257377.1:p.Lys431Ile
XM_006721516.2:c.1520A>T XP_006721579.2:p.Lys507Ile
XM_011523829.1:c.1435-90A>T XP_011522131.1:n.1435-90A>T
XM_011523830.1:c.1435-90A>T XP_011522132.1:n.1435-90A>T
XR_934021.1:n.1627A>T
XR_934022.1:n.1542-90A>T
XR_934023.1:n.1542-90A>T
XM_006721516.3:c.1520A>T XP_006721579.2:p.Lys507Ile
XM_011523829.2:c.1435-90A>T XP_011522131.1:n.1435-90A>T
XM_011523830.2:c.1435-90A>T XP_011522132.1:n.1435-90A>T
XM_024450741.1:c.1435-90A>T XP_024306509.1:n.1435-90A>T
XR_934021.2:n.1579A>T
XR_934022.2:n.1494-90A>T
XR_934023.2:n.1494-90A>T
NM_000018.4:c.1520A>T MANE Select NP_000009.1:p.Lys507Ile
NM_001033859.3:c.1454A>T NP_001029031.1:p.Lys485Ile
NM_001270447.2:c.1589A>T NP_001257376.1:p.Lys530Ile
NM_001270448.2:c.1292A>T NP_001257377.1:p.Lys431Ile