Canonical Allele Identifier: CA2245716401
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7225048C= , CM000679.2:g.7225048C= GRCh38
NC_000017.10:g.7128367C= , CM000679.1:g.7128367C= GRCh37
NC_000017.9:g.7069091C= NCBI36
NG_007975.1:g.10215C=
NG_008391.2:g.3G=
NG_033038.1:g.14497G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1919C= MANE Select ENSP00000349297.5:p.Ala640=
ENST00000322910.9:c.*1874C= ENSP00000325395.5:n.*1874C=
ENST00000350303.9:c.1853C= ENSP00000344152.5:p.Ala618=
ENST00000356839.9:c.1919C= ENSP00000349297.5:p.Ala640=
ENST00000542255.6:c.798C=
ENST00000543245.6:c.1988C= ENSP00000438689.2:p.Ala663=
ENST00000578033.1:n.344C=
ENST00000578319.5:n.500C=
ENST00000578711.1:n.1544C=
ENST00000578809.5:n.491C=
ENST00000579425.5:n.1035C=
ENST00000583848.5:c.285C= ENSP00000466487.1:n.285C=
ENST00000583850.5:n.690C=
ENST00000583858.5:c.850C=
NM_000018.3:c.1919C= NP_000009.1:p.Ala640=
NM_001033859.2:c.1853C= NP_001029031.1:p.Ala618=
NM_001270447.1:c.1988C= NP_001257376.1:p.Ala663=
NM_001270448.1:c.1691C= NP_001257377.1:p.Ala564=
XM_006721516.2:c.1940C= XP_006721579.2:p.Ala647=
XM_011523829.1:c.1838C= XP_011522131.1:p.Ala613=
XM_011523830.1:c.1817C= XP_011522132.1:p.Ala606=
XR_934021.1:n.2022C=
XR_934022.1:n.1928C=
XR_934023.1:n.1949C=
XM_006721516.3:c.1940C= XP_006721579.2:p.Ala647=
XM_011523829.2:c.1838C= XP_011522131.1:p.Ala613=
XM_011523830.2:c.1817C= XP_011522132.1:p.Ala606=
XM_024450741.1:c.1907C= XP_024306509.1:p.Ala636=
XR_934021.2:n.1974C=
XR_934022.2:n.1880C=
XR_934023.2:n.1901C=
NM_000018.4:c.1919C= MANE Select NP_000009.1:p.Ala640=
NM_001033859.3:c.1853C= NP_001029031.1:p.Ala618=
NM_001270447.2:c.1988C= NP_001257376.1:p.Ala663=
NM_001270448.2:c.1691C= NP_001257377.1:p.Ala564=