Canonical Allele Identifier: CA2245712801
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224055C= , CM000679.2:g.7224055C= GRCh38
NC_000017.10:g.7127374C= , CM000679.1:g.7127374C= GRCh37
NC_000017.9:g.7068098C= NCBI36
NG_007975.1:g.9222C=
NG_008391.2:g.996G=
NG_033038.1:g.15490G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1420C= MANE Select ENSP00000349297.5:p.Leu474=
ENST00000322910.9:c.*1375C= ENSP00000325395.5:n.*1375C=
ENST00000350303.9:c.1354C= ENSP00000344152.5:p.Leu452=
ENST00000356839.9:c.1420C= ENSP00000349297.5:p.Leu474=
ENST00000542255.6:c.278C=
ENST00000543245.6:c.1489C= ENSP00000438689.2:p.Leu497=
ENST00000578711.1:n.551C=
ENST00000579425.5:n.536C=
ENST00000579546.1:c.257C=
ENST00000579894.5:n.131C=
ENST00000583074.5:n.139C=
ENST00000583850.5:n.195C=
ENST00000583858.5:c.449C=
ENST00000585203.6:n.611C=
NM_000018.3:c.1420C= NP_000009.1:p.Leu474=
NM_001033859.2:c.1354C= NP_001029031.1:p.Leu452=
NM_001270447.1:c.1489C= NP_001257376.1:p.Leu497=
NM_001270448.1:c.1192C= NP_001257377.1:p.Leu398=
XM_006721516.2:c.1420C= XP_006721579.2:p.Leu474=
XM_011523829.1:c.1420C= XP_011522131.1:p.Leu474=
XM_011523830.1:c.1420C= XP_011522132.1:p.Leu474=
XR_934021.1:n.1527C=
XR_934022.1:n.1527C=
XR_934023.1:n.1527C=
XM_006721516.3:c.1420C= XP_006721579.2:p.Leu474=
XM_011523829.2:c.1420C= XP_011522131.1:p.Leu474=
XM_011523830.2:c.1420C= XP_011522132.1:p.Leu474=
XM_024450741.1:c.1420C= XP_024306509.1:p.Leu474=
XR_934021.2:n.1479C=
XR_934022.2:n.1479C=
XR_934023.2:n.1479C=
NM_000018.4:c.1420C= MANE Select NP_000009.1:p.Leu474=
NM_001033859.3:c.1354C= NP_001029031.1:p.Leu452=
NM_001270447.2:c.1489C= NP_001257376.1:p.Leu497=
NM_001270448.2:c.1192C= NP_001257377.1:p.Leu398=