Canonical Allele Identifier: CA2245711994
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223847A= , CM000679.2:g.7223847A= GRCh38
NC_000017.10:g.7127166A= , CM000679.1:g.7127166A= GRCh37
NC_000017.9:g.7067890A= NCBI36
NG_007975.1:g.9014A=
NG_008391.2:g.1204T=
NG_033038.1:g.15698T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1304A= MANE Select ENSP00000349297.5:p.Gln435=
ENST00000322910.9:c.*1259A= ENSP00000325395.5:n.*1259A=
ENST00000350303.9:c.1238A= ENSP00000344152.5:p.Gln413=
ENST00000356839.9:c.1304A= ENSP00000349297.5:p.Gln435=
ENST00000542255.6:c.162A=
ENST00000543245.6:c.1373A= ENSP00000438689.2:p.Gln458=
ENST00000578711.1:n.343A=
ENST00000578824.5:n.720A=
ENST00000579425.5:n.328A=
ENST00000579546.1:c.141A=
ENST00000583074.5:n.23A=
ENST00000583850.5:n.79A=
ENST00000583858.5:c.333A=
ENST00000585203.6:n.512A=
NM_000018.3:c.1304A= NP_000009.1:p.Gln435=
NM_001033859.2:c.1238A= NP_001029031.1:p.Gln413=
NM_001270447.1:c.1373A= NP_001257376.1:p.Gln458=
NM_001270448.1:c.1076A= NP_001257377.1:p.Gln359=
XM_006721516.2:c.1304A= XP_006721579.2:p.Gln435=
XM_011523829.1:c.1304A= XP_011522131.1:p.Gln435=
XM_011523830.1:c.1304A= XP_011522132.1:p.Gln435=
XR_934021.1:n.1411A=
XR_934022.1:n.1411A=
XR_934023.1:n.1411A=
XM_006721516.3:c.1304A= XP_006721579.2:p.Gln435=
XM_011523829.2:c.1304A= XP_011522131.1:p.Gln435=
XM_011523830.2:c.1304A= XP_011522132.1:p.Gln435=
XM_024450741.1:c.1304A= XP_024306509.1:p.Gln435=
XR_934021.2:n.1363A=
XR_934022.2:n.1363A=
XR_934023.2:n.1363A=
NM_000018.4:c.1304A= MANE Select NP_000009.1:p.Gln435=
NM_001033859.3:c.1238A= NP_001029031.1:p.Gln413=
NM_001270447.2:c.1373A= NP_001257376.1:p.Gln458=
NM_001270448.2:c.1076A= NP_001257377.1:p.Gln359=