Canonical Allele Identifier: CA2245712320
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223934G= , CM000679.2:g.7223934G= GRCh38
NC_000017.10:g.7127253G= , CM000679.1:g.7127253G= GRCh37
NC_000017.9:g.7067977G= NCBI36
NG_007975.1:g.9101G=
NG_008391.2:g.1117C=
NG_033038.1:g.15611C=

Transcript Alleles

HGVS Amino-acid change
ENST00000356839.10:c.1333-34G= MANE Select ENSP00000349297.5:n.1333-34G=
ENST00000322910.9:c.*1288-34G= ENSP00000325395.5:n.*1288-34G=
ENST00000350303.9:c.1267-34G= ENSP00000344152.5:n.1267-34G=
ENST00000356839.9:c.1333-34G= ENSP00000349297.5:n.1333-34G=
ENST00000542255.6:c.191-34G=
ENST00000543245.6:c.1402-34G= ENSP00000438689.2:n.1402-34G=
ENST00000578711.1:n.430G=
ENST00000579425.5:n.415G=
ENST00000579546.1:c.170-34G=
ENST00000579894.5:n.10G=
ENST00000583074.5:n.52-34G=
ENST00000583850.5:n.108-34G=
ENST00000583858.5:c.362-34G=
ENST00000585203.6:n.524-34G=
NM_000018.3:c.1333-34G= NP_000009.1:n.1333-34G=
NM_001033859.2:c.1267-34G= NP_001029031.1:n.1267-34G=
NM_001270447.1:c.1402-34G= NP_001257376.1:n.1402-34G=
NM_001270448.1:c.1105-34G= NP_001257377.1:n.1105-34G=
XM_006721516.2:c.1333-34G= XP_006721579.2:n.1333-34G=
XM_011523829.1:c.1333-34G= XP_011522131.1:n.1333-34G=
XM_011523830.1:c.1333-34G= XP_011522132.1:n.1333-34G=
XR_934021.1:n.1440-34G=
XR_934022.1:n.1440-34G=
XR_934023.1:n.1440-34G=
XM_006721516.3:c.1333-34G= XP_006721579.2:n.1333-34G=
XM_011523829.2:c.1333-34G= XP_011522131.1:n.1333-34G=
XM_011523830.2:c.1333-34G= XP_011522132.1:n.1333-34G=
XM_024450741.1:c.1333-34G= XP_024306509.1:n.1333-34G=
XR_934021.2:n.1392-34G=
XR_934022.2:n.1392-34G=
XR_934023.2:n.1392-34G=
NM_000018.4:c.1333-34G= MANE Select NP_000009.1:n.1333-34G=
NM_001033859.3:c.1267-34G= NP_001029031.1:n.1267-34G=
NM_001270447.2:c.1402-34G= NP_001257376.1:n.1402-34G=
NM_001270448.2:c.1105-34G= NP_001257377.1:n.1105-34G=