Canonical Allele Identifier: CA2245714416
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224488G= , CM000679.2:g.7224488G= GRCh38
NC_000017.10:g.7127807G= , CM000679.1:g.7127807G= GRCh37
NC_000017.9:g.7068531G= NCBI36
NG_007975.1:g.9655G=
NG_008391.2:g.563C=
NG_033038.1:g.15057C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1614G= MANE Select ENSP00000349297.5:p.Arg538=
ENST00000322910.9:c.*1569G= ENSP00000325395.5:n.*1569G=
ENST00000350303.9:c.1548G= ENSP00000344152.5:p.Arg516=
ENST00000356839.9:c.1614G= ENSP00000349297.5:p.Arg538=
ENST00000542255.6:c.472G=
ENST00000543245.6:c.1683G= ENSP00000438689.2:p.Arg561=
ENST00000578319.5:n.195G=
ENST00000578711.1:n.984G=
ENST00000578809.5:n.186G=
ENST00000579391.1:n.218G=
ENST00000579425.5:n.730G=
ENST00000579546.1:c.349G=
ENST00000579894.5:n.401G=
ENST00000582450.1:n.122G=
ENST00000583074.5:n.235G=
ENST00000583850.5:n.385G=
ENST00000583858.5:c.545G=
ENST00000585203.6:n.805G=
NM_000018.3:c.1614G= NP_000009.1:p.Arg538=
NM_001033859.2:c.1548G= NP_001029031.1:p.Arg516=
NM_001270447.1:c.1683G= NP_001257376.1:p.Arg561=
NM_001270448.1:c.1386G= NP_001257377.1:p.Arg462=
XM_006721516.2:c.1614G= XP_006721579.2:p.Arg538=
XM_011523829.1:c.1512G= XP_011522131.1:p.Arg504=
XM_011523830.1:c.1512G= XP_011522132.1:p.Arg504=
XR_934021.1:n.1717G=
XR_934022.1:n.1623G=
XR_934023.1:n.1623G=
XM_006721516.3:c.1614G= XP_006721579.2:p.Arg538=
XM_011523829.2:c.1512G= XP_011522131.1:p.Arg504=
XM_011523830.2:c.1512G= XP_011522132.1:p.Arg504=
XM_024450741.1:c.1602G= XP_024306509.1:p.Arg534=
XR_934021.2:n.1669G=
XR_934022.2:n.1575G=
XR_934023.2:n.1575G=
NM_000018.4:c.1614G= MANE Select NP_000009.1:p.Arg538=
NM_001033859.3:c.1548G= NP_001029031.1:p.Arg516=
NM_001270447.2:c.1683G= NP_001257376.1:p.Arg561=
NM_001270448.2:c.1386G= NP_001257377.1:p.Arg462=