Canonical Allele Identifier: CA2245711984
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223842C= , CM000679.2:g.7223842C= GRCh38
NC_000017.10:g.7127161C= , CM000679.1:g.7127161C= GRCh37
NC_000017.9:g.7067885C= NCBI36
NG_007975.1:g.9009C=
NG_008391.2:g.1209G=
NG_033038.1:g.15703G=

Transcript Alleles

HGVS Amino-acid change
ENST00000356839.10:c.1299C= MANE Select ENSP00000349297.5:p.Cys433=
ENST00000322910.9:c.*1254C= ENSP00000325395.5:n.*1254C=
ENST00000350303.9:c.1233C= ENSP00000344152.5:p.Cys411=
ENST00000356839.9:c.1299C= ENSP00000349297.5:p.Cys433=
ENST00000542255.6:c.157C=
ENST00000543245.6:c.1368C= ENSP00000438689.2:p.Cys456=
ENST00000578711.1:n.338C=
ENST00000578824.5:n.715C=
ENST00000579425.5:n.323C=
ENST00000579546.1:c.136C=
ENST00000583074.5:n.18C=
ENST00000583850.5:n.74C=
ENST00000583858.5:c.328C=
ENST00000585203.6:n.507C=
NM_000018.3:c.1299C= NP_000009.1:p.Cys433=
NM_001033859.2:c.1233C= NP_001029031.1:p.Cys411=
NM_001270447.1:c.1368C= NP_001257376.1:p.Cys456=
NM_001270448.1:c.1071C= NP_001257377.1:p.Cys357=
XM_006721516.2:c.1299C= XP_006721579.2:p.Cys433=
XM_011523829.1:c.1299C= XP_011522131.1:p.Cys433=
XM_011523830.1:c.1299C= XP_011522132.1:p.Cys433=
XR_934021.1:n.1406C=
XR_934022.1:n.1406C=
XR_934023.1:n.1406C=
XM_006721516.3:c.1299C= XP_006721579.2:p.Cys433=
XM_011523829.2:c.1299C= XP_011522131.1:p.Cys433=
XM_011523830.2:c.1299C= XP_011522132.1:p.Cys433=
XM_024450741.1:c.1299C= XP_024306509.1:p.Cys433=
XR_934021.2:n.1358C=
XR_934022.2:n.1358C=
XR_934023.2:n.1358C=
NM_000018.4:c.1299C= MANE Select NP_000009.1:p.Cys433=
NM_001033859.3:c.1233C= NP_001029031.1:p.Cys411=
NM_001270447.2:c.1368C= NP_001257376.1:p.Cys456=
NM_001270448.2:c.1071C= NP_001257377.1:p.Cys357=