Canonical Allele Identifier: CA2245714540
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224530A= , CM000679.2:g.7224530A= GRCh38
NC_000017.10:g.7127849A= , CM000679.1:g.7127849A= GRCh37
NC_000017.9:g.7068573A= NCBI36
NG_007975.1:g.9697A=
NG_008391.2:g.521T=
NG_033038.1:g.15015T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1656A= MANE Select ENSP00000349297.5:p.Ile552=
ENST00000322910.9:c.*1611A= ENSP00000325395.5:n.*1611A=
ENST00000350303.9:c.1590A= ENSP00000344152.5:p.Ile530=
ENST00000356839.9:c.1656A= ENSP00000349297.5:p.Ile552=
ENST00000542255.6:c.514A=
ENST00000543245.6:c.1725A= ENSP00000438689.2:p.Ile575=
ENST00000578319.5:n.237A=
ENST00000578711.1:n.1026A=
ENST00000578809.5:n.228A=
ENST00000579391.1:n.260A=
ENST00000579425.5:n.772A=
ENST00000579546.1:c.391A=
ENST00000582450.1:n.164A=
ENST00000583074.5:n.277A=
ENST00000583848.5:c.42A= ENSP00000466487.1:p.Ile14=
ENST00000583850.5:n.427A=
ENST00000583858.5:c.587A=
ENST00000585203.6:n.847A=
NM_000018.3:c.1656A= NP_000009.1:p.Ile552=
NM_001033859.2:c.1590A= NP_001029031.1:p.Ile530=
NM_001270447.1:c.1725A= NP_001257376.1:p.Ile575=
NM_001270448.1:c.1428A= NP_001257377.1:p.Ile476=
XM_006721516.2:c.1656A= XP_006721579.2:p.Ile552=
XM_011523829.1:c.1554A= XP_011522131.1:p.Ile518=
XM_011523830.1:c.1554A= XP_011522132.1:p.Ile518=
XR_934021.1:n.1759A=
XR_934022.1:n.1665A=
XR_934023.1:n.1665A=
XM_006721516.3:c.1656A= XP_006721579.2:p.Ile552=
XM_011523829.2:c.1554A= XP_011522131.1:p.Ile518=
XM_011523830.2:c.1554A= XP_011522132.1:p.Ile518=
XM_024450741.1:c.1644A= XP_024306509.1:p.Ile548=
XR_934021.2:n.1711A=
XR_934022.2:n.1617A=
XR_934023.2:n.1617A=
NM_000018.4:c.1656A= MANE Select NP_000009.1:p.Ile552=
NM_001033859.3:c.1590A= NP_001029031.1:p.Ile530=
NM_001270447.2:c.1725A= NP_001257376.1:p.Ile575=
NM_001270448.2:c.1428A= NP_001257377.1:p.Ile476=