Canonical Allele Identifier: CA2245716404
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7225050T= , CM000679.2:g.7225050T= GRCh38
NC_000017.10:g.7128369T= , CM000679.1:g.7128369T= GRCh37
NC_000017.9:g.7069093T= NCBI36
NG_007975.1:g.10217T=
NG_008391.2:g.1A=
NG_033038.1:g.14495A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1921T= MANE Select ENSP00000349297.5:p.Leu641=
ENST00000322910.9:c.*1876T= ENSP00000325395.5:n.*1876T=
ENST00000350303.9:c.1855T= ENSP00000344152.5:p.Leu619=
ENST00000356839.9:c.1921T= ENSP00000349297.5:p.Leu641=
ENST00000542255.6:c.800T=
ENST00000543245.6:c.1990T= ENSP00000438689.2:p.Leu664=
ENST00000578033.1:n.346T=
ENST00000578319.5:n.502T=
ENST00000578711.1:n.1546T=
ENST00000578809.5:n.493T=
ENST00000579425.5:n.1037T=
ENST00000583848.5:c.287T= ENSP00000466487.1:n.287T=
ENST00000583850.5:n.692T=
ENST00000583858.5:c.852T=
NM_000018.3:c.1921T= NP_000009.1:p.Leu641=
NM_001033859.2:c.1855T= NP_001029031.1:p.Leu619=
NM_001270447.1:c.1990T= NP_001257376.1:p.Leu664=
NM_001270448.1:c.1693T= NP_001257377.1:p.Leu565=
XM_006721516.2:c.1942T= XP_006721579.2:p.Leu648=
XM_011523829.1:c.1840T= XP_011522131.1:p.Leu614=
XM_011523830.1:c.1819T= XP_011522132.1:p.Leu607=
XR_934021.1:n.2024T=
XR_934022.1:n.1930T=
XR_934023.1:n.1951T=
XM_006721516.3:c.1942T= XP_006721579.2:p.Leu648=
XM_011523829.2:c.1840T= XP_011522131.1:p.Leu614=
XM_011523830.2:c.1819T= XP_011522132.1:p.Leu607=
XM_024450741.1:c.1909T= XP_024306509.1:p.Leu637=
XR_934021.2:n.1976T=
XR_934022.2:n.1882T=
XR_934023.2:n.1903T=
NM_000018.4:c.1921T= MANE Select NP_000009.1:p.Leu641=
NM_001033859.3:c.1855T= NP_001029031.1:p.Leu619=
NM_001270447.2:c.1990T= NP_001257376.1:p.Leu664=
NM_001270448.2:c.1693T= NP_001257377.1:p.Leu565=