Canonical Allele Identifier: CA2245713197
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224157G= , CM000679.2:g.7224157G= GRCh38
NC_000017.10:g.7127476G= , CM000679.1:g.7127476G= GRCh37
NC_000017.9:g.7068200G= NCBI36
NG_007975.1:g.9324G=
NG_008391.2:g.894C=
NG_033038.1:g.15388C=

Transcript Alleles

HGVS Amino-acid change
ENST00000356839.10:c.1446G= MANE Select ENSP00000349297.5:p.Lys482=
ENST00000322910.9:c.*1401G= ENSP00000325395.5:n.*1401G=
ENST00000350303.9:c.1380G= ENSP00000344152.5:p.Lys460=
ENST00000356839.9:c.1446G= ENSP00000349297.5:p.Lys482=
ENST00000542255.6:c.304G=
ENST00000543245.6:c.1515G= ENSP00000438689.2:p.Lys505=
ENST00000578711.1:n.653G=
ENST00000579391.1:n.54G=
ENST00000579425.5:n.562G=
ENST00000579546.1:c.271+88G=
ENST00000579894.5:n.233G=
ENST00000583074.5:n.153+88G=
ENST00000583850.5:n.221G=
ENST00000583858.5:c.463+88G=
ENST00000585203.6:n.637G=
NM_000018.3:c.1446G= NP_000009.1:p.Lys482=
NM_001033859.2:c.1380G= NP_001029031.1:p.Lys460=
NM_001270447.1:c.1515G= NP_001257376.1:p.Lys505=
NM_001270448.1:c.1218G= NP_001257377.1:p.Lys406=
XM_006721516.2:c.1446G= XP_006721579.2:p.Lys482=
XM_011523829.1:c.1434+88G= XP_011522131.1:n.1434+88G=
XM_011523830.1:c.1434+88G= XP_011522132.1:n.1434+88G=
XR_934021.1:n.1553G=
XR_934022.1:n.1541+88G=
XR_934023.1:n.1541+88G=
XM_006721516.3:c.1446G= XP_006721579.2:p.Lys482=
XM_011523829.2:c.1434+88G= XP_011522131.1:n.1434+88G=
XM_011523830.2:c.1434+88G= XP_011522132.1:n.1434+88G=
XM_024450741.1:c.1434+88G= XP_024306509.1:n.1434+88G=
XR_934021.2:n.1505G=
XR_934022.2:n.1493+88G=
XR_934023.2:n.1493+88G=
NM_000018.4:c.1446G= MANE Select NP_000009.1:p.Lys482=
NM_001033859.3:c.1380G= NP_001029031.1:p.Lys460=
NM_001270447.2:c.1515G= NP_001257376.1:p.Lys505=
NM_001270448.2:c.1218G= NP_001257377.1:p.Lys406=