Canonical Allele Identifier: CA2245716395
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7225044A= , CM000679.2:g.7225044A= GRCh38
NC_000017.10:g.7128363A= , CM000679.1:g.7128363A= GRCh37
NC_000017.9:g.7069087A= NCBI36
NG_007975.1:g.10211A=
NG_008391.2:g.7T=
NG_033038.1:g.14501T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1915A= MANE Select ENSP00000349297.5:p.Lys639=
ENST00000322910.9:c.*1870A= ENSP00000325395.5:n.*1870A=
ENST00000350303.9:c.1849A= ENSP00000344152.5:p.Lys617=
ENST00000356839.9:c.1915A= ENSP00000349297.5:p.Lys639=
ENST00000542255.6:c.794A=
ENST00000543245.6:c.1984A= ENSP00000438689.2:p.Lys662=
ENST00000578033.1:n.340A=
ENST00000578319.5:n.496A=
ENST00000578711.1:n.1540A=
ENST00000578809.5:n.487A=
ENST00000579425.5:n.1031A=
ENST00000583848.5:c.281A= ENSP00000466487.1:n.281A=
ENST00000583850.5:n.686A=
ENST00000583858.5:c.846A=
NM_000018.3:c.1915A= NP_000009.1:p.Lys639=
NM_001033859.2:c.1849A= NP_001029031.1:p.Lys617=
NM_001270447.1:c.1984A= NP_001257376.1:p.Lys662=
NM_001270448.1:c.1687A= NP_001257377.1:p.Lys563=
XM_006721516.2:c.1936A= XP_006721579.2:p.Lys646=
XM_011523829.1:c.1834A= XP_011522131.1:p.Lys612=
XM_011523830.1:c.1813A= XP_011522132.1:p.Lys605=
XR_934021.1:n.2018A=
XR_934022.1:n.1924A=
XR_934023.1:n.1945A=
XM_006721516.3:c.1936A= XP_006721579.2:p.Lys646=
XM_011523829.2:c.1834A= XP_011522131.1:p.Lys612=
XM_011523830.2:c.1813A= XP_011522132.1:p.Lys605=
XM_024450741.1:c.1903A= XP_024306509.1:p.Lys635=
XR_934021.2:n.1970A=
XR_934022.2:n.1876A=
XR_934023.2:n.1897A=
NM_000018.4:c.1915A= MANE Select NP_000009.1:p.Lys639=
NM_001033859.3:c.1849A= NP_001029031.1:p.Lys617=
NM_001270447.2:c.1984A= NP_001257376.1:p.Lys662=
NM_001270448.2:c.1687A= NP_001257377.1:p.Lys563=