Canonical Allele Identifier: CA2245700448
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221672G= , CM000679.2:g.7221672G= GRCh38
NC_000017.10:g.7124991G= , CM000679.1:g.7124991G= GRCh37
NC_000017.9:g.7065715G= NCBI36
NG_007975.1:g.6839G=
NG_008391.2:g.3379C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.612G= MANE Select ENSP00000349297.5:p.Lys204=
ENST00000322910.9:c.*567G= ENSP00000325395.5:n.*567G=
ENST00000350303.9:c.546G= ENSP00000344152.5:p.Lys182=
ENST00000356839.9:c.612G= ENSP00000349297.5:p.Lys204=
ENST00000543245.6:c.681G= ENSP00000438689.2:p.Lys227=
ENST00000577191.5:n.689G=
ENST00000577857.5:n.428G=
ENST00000579286.5:n.793G=
ENST00000579886.2:c.450G= ENSP00000463246.1:p.Lys150=
ENST00000580365.1:n.343G=
ENST00000581378.5:c.330G=
ENST00000581562.5:n.525-280G=
ENST00000583312.5:c.612G= ENSP00000467920.1:p.Lys204=
ENST00000583760.1:n.394G=
NM_000018.3:c.612G= NP_000009.1:p.Lys204=
NM_001033859.2:c.546G= NP_001029031.1:p.Lys182=
NM_001270447.1:c.681G= NP_001257376.1:p.Lys227=
NM_001270448.1:c.384G= NP_001257377.1:p.Lys128=
XM_006721516.2:c.612G= XP_006721579.2:p.Lys204=
XM_011523829.1:c.612G= XP_011522131.1:p.Lys204=
XM_011523830.1:c.612G= XP_011522132.1:p.Lys204=
XR_934021.1:n.719G=
XR_934022.1:n.719G=
XR_934023.1:n.719G=
XM_006721516.3:c.612G= XP_006721579.2:p.Lys204=
XM_011523829.2:c.612G= XP_011522131.1:p.Lys204=
XM_011523830.2:c.612G= XP_011522132.1:p.Lys204=
XM_024450741.1:c.612G= XP_024306509.1:p.Lys204=
XR_934021.2:n.671G=
XR_934022.2:n.671G=
XR_934023.2:n.671G=
NM_000018.4:c.612G= MANE Select NP_000009.1:p.Lys204=
NM_001033859.3:c.546G= NP_001029031.1:p.Lys182=
NM_001270447.2:c.681G= NP_001257376.1:p.Lys227=
NM_001270448.2:c.384G= NP_001257377.1:p.Lys128=