Canonical Allele Identifier: CA2245713651
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224286G= , CM000679.2:g.7224286G= GRCh38
NC_000017.10:g.7127605G= , CM000679.1:g.7127605G= GRCh37
NC_000017.9:g.7068329G= NCBI36
NG_007975.1:g.9453G=
NG_008391.2:g.765C=
NG_033038.1:g.15259C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1533-35G= MANE Select ENSP00000349297.5:n.1533-35G=
ENST00000322910.9:c.*1488-35G= ENSP00000325395.5:n.*1488-35G=
ENST00000350303.9:c.1467-35G= ENSP00000344152.5:n.1467-35G=
ENST00000356839.9:c.1533-35G= ENSP00000349297.5:n.1533-35G=
ENST00000542255.6:c.391-35G=
ENST00000543245.6:c.1602-35G= ENSP00000438689.2:n.1602-35G=
ENST00000578319.5:n.28-35G=
ENST00000578711.1:n.782G=
ENST00000578809.5:n.70G=
ENST00000579391.1:n.141-35G=
ENST00000579425.5:n.649-35G=
ENST00000579546.1:c.272-35G=
ENST00000579894.5:n.320-35G=
ENST00000582450.1:n.6G=
ENST00000583074.5:n.154-35G=
ENST00000583850.5:n.308-35G=
ENST00000583858.5:c.464-35G=
ENST00000585203.6:n.724-35G=
NM_000018.3:c.1533-35G= NP_000009.1:n.1533-35G=
NM_001033859.2:c.1467-35G= NP_001029031.1:n.1467-35G=
NM_001270447.1:c.1602-35G= NP_001257376.1:n.1602-35G=
NM_001270448.1:c.1305-35G= NP_001257377.1:n.1305-35G=
XM_006721516.2:c.1533-35G= XP_006721579.2:n.1533-35G=
XM_011523829.1:c.1435-35G= XP_011522131.1:n.1435-35G=
XM_011523830.1:c.1435-35G= XP_011522132.1:n.1435-35G=
XR_934021.1:n.1640-35G=
XR_934022.1:n.1542-35G=
XR_934023.1:n.1542-35G=
XM_006721516.3:c.1533-35G= XP_006721579.2:n.1533-35G=
XM_011523829.2:c.1435-35G= XP_011522131.1:n.1435-35G=
XM_011523830.2:c.1435-35G= XP_011522132.1:n.1435-35G=
XM_024450741.1:c.1435-35G= XP_024306509.1:n.1435-35G=
XR_934021.2:n.1592-35G=
XR_934022.2:n.1494-35G=
XR_934023.2:n.1494-35G=
NM_000018.4:c.1533-35G= MANE Select NP_000009.1:n.1533-35G=
NM_001033859.3:c.1467-35G= NP_001029031.1:n.1467-35G=
NM_001270447.2:c.1602-35G= NP_001257376.1:n.1602-35G=
NM_001270448.2:c.1305-35G= NP_001257377.1:n.1305-35G=