Canonical Allele Identifier: CA2245712367
Gene: ACADVL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223962T= , CM000679.2:g.7223962T= GRCh38
NC_000017.10:g.7127281T= , CM000679.1:g.7127281T= GRCh37
NC_000017.9:g.7068005T= NCBI36
NG_007975.1:g.9129T=
NG_008391.2:g.1089A=
NG_033038.1:g.15583A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1333-6T= MANE Select ENSP00000349297.5:n.1333-6T=
ENST00000322910.9:c.*1288-6T= ENSP00000325395.5:n.*1288-6T=
ENST00000350303.9:c.1267-6T= ENSP00000344152.5:n.1267-6T=
ENST00000356839.9:c.1333-6T= ENSP00000349297.5:n.1333-6T=
ENST00000542255.6:c.191-6T=
ENST00000543245.6:c.1402-6T= ENSP00000438689.2:n.1402-6T=
ENST00000578711.1:n.458T=
ENST00000579425.5:n.443T=
ENST00000579546.1:c.170-6T=
ENST00000579894.5:n.38T=
ENST00000583074.5:n.52-6T=
ENST00000583850.5:n.108-6T=
ENST00000583858.5:c.362-6T=
ENST00000585203.6:n.524-6T=
NM_000018.3:c.1333-6T= NP_000009.1:n.1333-6T=
NM_001033859.2:c.1267-6T= NP_001029031.1:n.1267-6T=
NM_001270447.1:c.1402-6T= NP_001257376.1:n.1402-6T=
NM_001270448.1:c.1105-6T= NP_001257377.1:n.1105-6T=
XM_006721516.2:c.1333-6T= XP_006721579.2:n.1333-6T=
XM_011523829.1:c.1333-6T= XP_011522131.1:n.1333-6T=
XM_011523830.1:c.1333-6T= XP_011522132.1:n.1333-6T=
XR_934021.1:n.1440-6T=
XR_934022.1:n.1440-6T=
XR_934023.1:n.1440-6T=
XM_006721516.3:c.1333-6T= XP_006721579.2:n.1333-6T=
XM_011523829.2:c.1333-6T= XP_011522131.1:n.1333-6T=
XM_011523830.2:c.1333-6T= XP_011522132.1:n.1333-6T=
XM_024450741.1:c.1333-6T= XP_024306509.1:n.1333-6T=
XR_934021.2:n.1392-6T=
XR_934022.2:n.1392-6T=
XR_934023.2:n.1392-6T=
NM_000018.4:c.1333-6T= MANE Select NP_000009.1:n.1333-6T=
NM_001033859.3:c.1267-6T= NP_001029031.1:n.1267-6T=
NM_001270447.2:c.1402-6T= NP_001257376.1:n.1402-6T=
NM_001270448.2:c.1105-6T= NP_001257377.1:n.1105-6T=
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