Canonical Allele Identifier: CA2245700832
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221979C= , CM000679.2:g.7221979C= GRCh38
NC_000017.10:g.7125298C= , CM000679.1:g.7125298C= GRCh37
NC_000017.9:g.7066022C= NCBI36
NG_007975.1:g.7146C=
NG_008391.2:g.3072G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.650C= MANE Select ENSP00000349297.5:p.Thr217=
ENST00000322910.9:c.*605C= ENSP00000325395.5:n.*605C=
ENST00000350303.9:c.584C= ENSP00000344152.5:p.Thr195=
ENST00000356839.9:c.650C= ENSP00000349297.5:p.Thr217=
ENST00000543245.6:c.719C= ENSP00000438689.2:p.Thr240=
ENST00000577191.5:n.727C=
ENST00000577857.5:n.466C=
ENST00000579286.5:n.831C=
ENST00000580365.1:n.381C=
ENST00000581378.5:c.368C=
ENST00000581562.5:n.552C=
ENST00000582379.1:n.34C=
ENST00000583312.5:c.665C= ENSP00000467920.1:p.Thr222=
ENST00000583760.1:n.432C=
NM_000018.3:c.650C= NP_000009.1:p.Thr217=
NM_001033859.2:c.584C= NP_001029031.1:p.Thr195=
NM_001270447.1:c.719C= NP_001257376.1:p.Thr240=
NM_001270448.1:c.422C= NP_001257377.1:p.Thr141=
XM_006721516.2:c.650C= XP_006721579.2:p.Thr217=
XM_011523829.1:c.650C= XP_011522131.1:p.Thr217=
XM_011523830.1:c.650C= XP_011522132.1:p.Thr217=
XR_934021.1:n.757C=
XR_934022.1:n.757C=
XR_934023.1:n.757C=
XM_006721516.3:c.650C= XP_006721579.2:p.Thr217=
XM_011523829.2:c.650C= XP_011522131.1:p.Thr217=
XM_011523830.2:c.650C= XP_011522132.1:p.Thr217=
XM_024450741.1:c.650C= XP_024306509.1:p.Thr217=
XR_934021.2:n.709C=
XR_934022.2:n.709C=
XR_934023.2:n.709C=
NM_000018.4:c.650C= MANE Select NP_000009.1:p.Thr217=
NM_001033859.3:c.584C= NP_001029031.1:p.Thr195=
NM_001270447.2:c.719C= NP_001257376.1:p.Thr240=
NM_001270448.2:c.422C= NP_001257377.1:p.Thr141=