Canonical Allele Identifier: CA2245712875
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224080G= , CM000679.2:g.7224080G= GRCh38
NC_000017.10:g.7127399G= , CM000679.1:g.7127399G= GRCh37
NC_000017.9:g.7068123G= NCBI36
NG_007975.1:g.9247G=
NG_008391.2:g.971C=
NG_033038.1:g.15465C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1434+11G= MANE Select ENSP00000349297.5:n.1434+11G=
ENST00000322910.9:c.*1389+11G= ENSP00000325395.5:n.*1389+11G=
ENST00000350303.9:c.1368+11G= ENSP00000344152.5:n.1368+11G=
ENST00000356839.9:c.1434+11G= ENSP00000349297.5:n.1434+11G=
ENST00000542255.6:c.292+11G=
ENST00000543245.6:c.1503+11G= ENSP00000438689.2:n.1503+11G=
ENST00000578711.1:n.576G=
ENST00000579425.5:n.550+11G=
ENST00000579546.1:c.271+11G=
ENST00000579894.5:n.156G=
ENST00000583074.5:n.153+11G=
ENST00000583850.5:n.209+11G=
ENST00000583858.5:c.463+11G=
ENST00000585203.6:n.625+11G=
NM_000018.3:c.1434+11G= NP_000009.1:n.1434+11G=
NM_001033859.2:c.1368+11G= NP_001029031.1:n.1368+11G=
NM_001270447.1:c.1503+11G= NP_001257376.1:n.1503+11G=
NM_001270448.1:c.1206+11G= NP_001257377.1:n.1206+11G=
XM_006721516.2:c.1434+11G= XP_006721579.2:n.1434+11G=
XM_011523829.1:c.1434+11G= XP_011522131.1:n.1434+11G=
XM_011523830.1:c.1434+11G= XP_011522132.1:n.1434+11G=
XR_934021.1:n.1541+11G=
XR_934022.1:n.1541+11G=
XR_934023.1:n.1541+11G=
XM_006721516.3:c.1434+11G= XP_006721579.2:n.1434+11G=
XM_011523829.2:c.1434+11G= XP_011522131.1:n.1434+11G=
XM_011523830.2:c.1434+11G= XP_011522132.1:n.1434+11G=
XM_024450741.1:c.1434+11G= XP_024306509.1:n.1434+11G=
XR_934021.2:n.1493+11G=
XR_934022.2:n.1493+11G=
XR_934023.2:n.1493+11G=
NM_000018.4:c.1434+11G= MANE Select NP_000009.1:n.1434+11G=
NM_001033859.3:c.1368+11G= NP_001029031.1:n.1368+11G=
NM_001270447.2:c.1503+11G= NP_001257376.1:n.1503+11G=
NM_001270448.2:c.1206+11G= NP_001257377.1:n.1206+11G=