Canonical Allele Identifier: CA2245700871
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221995G= , CM000679.2:g.7221995G= GRCh38
NC_000017.10:g.7125314G= , CM000679.1:g.7125314G= GRCh37
NC_000017.9:g.7066038G= NCBI36
NG_007975.1:g.7162G=
NG_008391.2:g.3056C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.666G= MANE Select ENSP00000349297.5:p.Gly222=
ENST00000322910.9:c.*621G= ENSP00000325395.5:n.*621G=
ENST00000350303.9:c.600G= ENSP00000344152.5:p.Gly200=
ENST00000356839.9:c.666G= ENSP00000349297.5:p.Gly222=
ENST00000543245.6:c.735G= ENSP00000438689.2:p.Gly245=
ENST00000577191.5:n.743G=
ENST00000577857.5:n.482G=
ENST00000579286.5:n.847G=
ENST00000580365.1:n.397G=
ENST00000581378.5:c.384G=
ENST00000581562.5:n.568G=
ENST00000582379.1:n.50G=
ENST00000583760.1:n.448G=
NM_000018.3:c.666G= NP_000009.1:p.Gly222=
NM_001033859.2:c.600G= NP_001029031.1:p.Gly200=
NM_001270447.1:c.735G= NP_001257376.1:p.Gly245=
NM_001270448.1:c.438G= NP_001257377.1:p.Gly146=
XM_006721516.2:c.666G= XP_006721579.2:p.Gly222=
XM_011523829.1:c.666G= XP_011522131.1:p.Gly222=
XM_011523830.1:c.666G= XP_011522132.1:p.Gly222=
XR_934021.1:n.773G=
XR_934022.1:n.773G=
XR_934023.1:n.773G=
XM_006721516.3:c.666G= XP_006721579.2:p.Gly222=
XM_011523829.2:c.666G= XP_011522131.1:p.Gly222=
XM_011523830.2:c.666G= XP_011522132.1:p.Gly222=
XM_024450741.1:c.666G= XP_024306509.1:p.Gly222=
XR_934021.2:n.725G=
XR_934022.2:n.725G=
XR_934023.2:n.725G=
NM_000018.4:c.666G= MANE Select NP_000009.1:p.Gly222=
NM_001033859.3:c.600G= NP_001029031.1:p.Gly200=
NM_001270447.2:c.735G= NP_001257376.1:p.Gly245=
NM_001270448.2:c.438G= NP_001257377.1:p.Gly146=