Canonical Allele Identifier: CA2245711943
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223827G= , CM000679.2:g.7223827G= GRCh38
NC_000017.10:g.7127146G= , CM000679.1:g.7127146G= GRCh37
NC_000017.9:g.7067870G= NCBI36
NG_007975.1:g.8994G=
NG_008391.2:g.1224C=
NG_033038.1:g.15718C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1284G= MANE Select ENSP00000349297.5:p.Lys428=
ENST00000322910.9:c.*1239G= ENSP00000325395.5:n.*1239G=
ENST00000350303.9:c.1218G= ENSP00000344152.5:p.Lys406=
ENST00000356839.9:c.1284G= ENSP00000349297.5:p.Lys428=
ENST00000542255.6:c.142G=
ENST00000543245.6:c.1353G= ENSP00000438689.2:p.Lys451=
ENST00000578579.2:n.455G=
ENST00000578711.1:n.323G=
ENST00000578824.5:n.700G=
ENST00000579425.5:n.308G=
ENST00000579546.1:c.121G=
ENST00000583074.5:n.3G=
ENST00000583850.5:n.59G=
ENST00000583858.5:c.313G=
ENST00000585203.6:n.492G=
NM_000018.3:c.1284G= NP_000009.1:p.Lys428=
NM_001033859.2:c.1218G= NP_001029031.1:p.Lys406=
NM_001270447.1:c.1353G= NP_001257376.1:p.Lys451=
NM_001270448.1:c.1056G= NP_001257377.1:p.Lys352=
XM_006721516.2:c.1284G= XP_006721579.2:p.Lys428=
XM_011523829.1:c.1284G= XP_011522131.1:p.Lys428=
XM_011523830.1:c.1284G= XP_011522132.1:p.Lys428=
XR_934021.1:n.1391G=
XR_934022.1:n.1391G=
XR_934023.1:n.1391G=
XM_006721516.3:c.1284G= XP_006721579.2:p.Lys428=
XM_011523829.2:c.1284G= XP_011522131.1:p.Lys428=
XM_011523830.2:c.1284G= XP_011522132.1:p.Lys428=
XM_024450741.1:c.1284G= XP_024306509.1:p.Lys428=
XR_934021.2:n.1343G=
XR_934022.2:n.1343G=
XR_934023.2:n.1343G=
NM_000018.4:c.1284G= MANE Select NP_000009.1:p.Lys428=
NM_001033859.3:c.1218G= NP_001029031.1:p.Lys406=
NM_001270447.2:c.1353G= NP_001257376.1:p.Lys451=
NM_001270448.2:c.1056G= NP_001257377.1:p.Lys352=