Canonical Allele Identifier: CA2245716531
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7225085A= , CM000679.2:g.7225085A= GRCh38
NC_000017.10:g.7128404A= , CM000679.1:g.7128404A= GRCh37
NC_000017.9:g.7069128A= NCBI36
NG_007975.1:g.10252A=
NG_033038.1:g.14460T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1956A= MANE Select ENSP00000349297.5:p.Pro652=
ENST00000322910.9:c.*1911A= ENSP00000325395.5:n.*1911A=
ENST00000350303.9:c.1890A= ENSP00000344152.5:p.Pro630=
ENST00000356839.9:c.1956A= ENSP00000349297.5:p.Pro652=
ENST00000542255.6:c.835A=
ENST00000543245.6:c.2025A= ENSP00000438689.2:p.Pro675=
ENST00000578033.1:n.381A=
ENST00000578319.5:n.537A=
ENST00000578711.1:n.1581A=
ENST00000578809.5:n.528A=
ENST00000579425.5:n.1072A=
ENST00000583848.5:c.322A= ENSP00000466487.1:n.322A=
ENST00000583850.5:n.727A=
ENST00000583858.5:c.887A=
NM_000018.3:c.1956A= NP_000009.1:p.Pro652=
NM_001033859.2:c.1890A= NP_001029031.1:p.Pro630=
NM_001270447.1:c.2025A= NP_001257376.1:p.Pro675=
NM_001270448.1:c.1728A= NP_001257377.1:p.Pro576=
XM_006721516.2:c.1977A= XP_006721579.2:p.Pro659=
XM_011523829.1:c.1875A= XP_011522131.1:p.Pro625=
XM_011523830.1:c.1854A= XP_011522132.1:p.Pro618=
XR_934021.1:n.2059A=
XR_934022.1:n.1965A=
XR_934023.1:n.1986A=
XM_006721516.3:c.1977A= XP_006721579.2:p.Pro659=
XM_011523829.2:c.1875A= XP_011522131.1:p.Pro625=
XM_011523830.2:c.1854A= XP_011522132.1:p.Pro618=
XM_024450741.1:c.1944A= XP_024306509.1:p.Pro648=
XR_934021.2:n.2011A=
XR_934022.2:n.1917A=
XR_934023.2:n.1938A=
NM_000018.4:c.1956A= MANE Select NP_000009.1:p.Pro652=
NM_001033859.3:c.1890A= NP_001029031.1:p.Pro630=
NM_001270447.2:c.2025A= NP_001257376.1:p.Pro675=
NM_001270448.2:c.1728A= NP_001257377.1:p.Pro576=