Canonical Allele Identifier: CA2245699368
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221058G= , CM000679.2:g.7221058G= GRCh38
NC_000017.10:g.7124377G= , CM000679.1:g.7124377G= GRCh37
NC_000017.9:g.7065101G= NCBI36
NG_007975.1:g.6225G=
NG_008391.2:g.3993C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.477G= MANE Select ENSP00000349297.5:p.Gln159=
ENST00000322910.9:c.*432G= ENSP00000325395.5:n.*432G=
ENST00000350303.9:c.411G= ENSP00000344152.5:p.Gln137=
ENST00000356839.9:c.477G= ENSP00000349297.5:p.Gln159=
ENST00000543245.6:c.546G= ENSP00000438689.2:p.Gln182=
ENST00000577191.5:n.554G=
ENST00000577433.5:n.685G=
ENST00000577857.5:n.293+228G=
ENST00000579286.5:n.658G=
ENST00000579886.2:c.315G= ENSP00000463246.1:p.Gln105=
ENST00000580365.1:n.208G=
ENST00000581378.5:c.176G=
ENST00000581562.5:n.524G=
ENST00000582056.5:n.660G=
ENST00000582166.1:n.458G=
ENST00000583312.5:c.477G= ENSP00000467920.1:p.Gln159=
NM_000018.3:c.477G= NP_000009.1:p.Gln159=
NM_001033859.2:c.411G= NP_001029031.1:p.Gln137=
NM_001270447.1:c.546G= NP_001257376.1:p.Gln182=
NM_001270448.1:c.249G= NP_001257377.1:p.Gln83=
XM_006721516.2:c.477G= XP_006721579.2:p.Gln159=
XM_011523829.1:c.477G= XP_011522131.1:p.Gln159=
XM_011523830.1:c.477G= XP_011522132.1:p.Gln159=
XR_934021.1:n.584G=
XR_934022.1:n.584G=
XR_934023.1:n.584G=
XM_006721516.3:c.477G= XP_006721579.2:p.Gln159=
XM_011523829.2:c.477G= XP_011522131.1:p.Gln159=
XM_011523830.2:c.477G= XP_011522132.1:p.Gln159=
XM_024450741.1:c.477G= XP_024306509.1:p.Gln159=
XR_934021.2:n.536G=
XR_934022.2:n.536G=
XR_934023.2:n.536G=
NM_000018.4:c.477G= MANE Select NP_000009.1:p.Gln159=
NM_001033859.3:c.411G= NP_001029031.1:p.Gln137=
NM_001270447.2:c.546G= NP_001257376.1:p.Gln182=
NM_001270448.2:c.249G= NP_001257377.1:p.Gln83=