Canonical Allele Identifier: CA2245715722
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224849C= , CM000679.2:g.7224849C= GRCh38
NC_000017.10:g.7128168C= , CM000679.1:g.7128168C= GRCh37
NC_000017.9:g.7068892C= NCBI36
NG_007975.1:g.10016C=
NG_008391.2:g.202G=
NG_033038.1:g.14696G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1792C= MANE Select ENSP00000349297.5:p.His598=
ENST00000322910.9:c.*1747C= ENSP00000325395.5:n.*1747C=
ENST00000350303.9:c.1726C= ENSP00000344152.5:p.His576=
ENST00000356839.9:c.1792C= ENSP00000349297.5:p.His598=
ENST00000542255.6:c.671C=
ENST00000543245.6:c.1861C= ENSP00000438689.2:p.His621=
ENST00000578033.1:n.217C=
ENST00000578319.5:n.373C=
ENST00000578711.1:n.1345C=
ENST00000578809.5:n.364C=
ENST00000579425.5:n.908C=
ENST00000579546.1:c.527C=
ENST00000583848.5:c.158C= ENSP00000466487.1:n.158C=
ENST00000583850.5:n.563C=
ENST00000583858.5:c.723C=
NM_000018.3:c.1792C= NP_000009.1:p.His598=
NM_001033859.2:c.1726C= NP_001029031.1:p.His576=
NM_001270447.1:c.1861C= NP_001257376.1:p.His621=
NM_001270448.1:c.1564C= NP_001257377.1:p.His522=
XM_006721516.2:c.1813C= XP_006721579.2:p.His605=
XM_011523829.1:c.1711C= XP_011522131.1:p.His571=
XM_011523830.1:c.1690C= XP_011522132.1:p.His564=
XR_934021.1:n.1895C=
XR_934022.1:n.1801C=
XR_934023.1:n.1822C=
XM_006721516.3:c.1813C= XP_006721579.2:p.His605=
XM_011523829.2:c.1711C= XP_011522131.1:p.His571=
XM_011523830.2:c.1690C= XP_011522132.1:p.His564=
XM_024450741.1:c.1780C= XP_024306509.1:p.His594=
XR_934021.2:n.1847C=
XR_934022.2:n.1753C=
XR_934023.2:n.1774C=
NM_000018.4:c.1792C= MANE Select NP_000009.1:p.His598=
NM_001033859.3:c.1726C= NP_001029031.1:p.His576=
NM_001270447.2:c.1861C= NP_001257376.1:p.His621=
NM_001270448.2:c.1564C= NP_001257377.1:p.His522=