Canonical Allele Identifier: CA2245716400
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7225045A= , CM000679.2:g.7225045A= GRCh38
NC_000017.10:g.7128364A= , CM000679.1:g.7128364A= GRCh37
NC_000017.9:g.7069088A= NCBI36
NG_007975.1:g.10212A=
NG_008391.2:g.6T=
NG_033038.1:g.14500T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1916A= MANE Select ENSP00000349297.5:p.Lys639=
ENST00000322910.9:c.*1871A= ENSP00000325395.5:n.*1871A=
ENST00000350303.9:c.1850A= ENSP00000344152.5:p.Lys617=
ENST00000356839.9:c.1916A= ENSP00000349297.5:p.Lys639=
ENST00000542255.6:c.795A=
ENST00000543245.6:c.1985A= ENSP00000438689.2:p.Lys662=
ENST00000578033.1:n.341A=
ENST00000578319.5:n.497A=
ENST00000578711.1:n.1541A=
ENST00000578809.5:n.488A=
ENST00000579425.5:n.1032A=
ENST00000583848.5:c.282A= ENSP00000466487.1:n.282A=
ENST00000583850.5:n.687A=
ENST00000583858.5:c.847A=
NM_000018.3:c.1916A= NP_000009.1:p.Lys639=
NM_001033859.2:c.1850A= NP_001029031.1:p.Lys617=
NM_001270447.1:c.1985A= NP_001257376.1:p.Lys662=
NM_001270448.1:c.1688A= NP_001257377.1:p.Lys563=
XM_006721516.2:c.1937A= XP_006721579.2:p.Lys646=
XM_011523829.1:c.1835A= XP_011522131.1:p.Lys612=
XM_011523830.1:c.1814A= XP_011522132.1:p.Lys605=
XR_934021.1:n.2019A=
XR_934022.1:n.1925A=
XR_934023.1:n.1946A=
XM_006721516.3:c.1937A= XP_006721579.2:p.Lys646=
XM_011523829.2:c.1835A= XP_011522131.1:p.Lys612=
XM_011523830.2:c.1814A= XP_011522132.1:p.Lys605=
XM_024450741.1:c.1904A= XP_024306509.1:p.Lys635=
XR_934021.2:n.1971A=
XR_934022.2:n.1877A=
XR_934023.2:n.1898A=
NM_000018.4:c.1916A= MANE Select NP_000009.1:p.Lys639=
NM_001033859.3:c.1850A= NP_001029031.1:p.Lys617=
NM_001270447.2:c.1985A= NP_001257376.1:p.Lys662=
NM_001270448.2:c.1688A= NP_001257377.1:p.Lys563=