Canonical Allele Identifier: CA2245709323
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222699C= , CM000679.2:g.7222699C= GRCh38
NC_000017.10:g.7126018C= , CM000679.1:g.7126018C= GRCh37
NC_000017.9:g.7066742C= NCBI36
NG_007975.1:g.7866C=
NG_008391.2:g.2352G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.911C= MANE Select ENSP00000349297.5:p.Ala304=
ENST00000322910.9:c.*866C= ENSP00000325395.5:n.*866C=
ENST00000350303.9:c.845C= ENSP00000344152.5:p.Ala282=
ENST00000356839.9:c.911C= ENSP00000349297.5:p.Ala304=
ENST00000543245.6:c.980C= ENSP00000438689.2:p.Ala327=
ENST00000578824.5:n.60C=
ENST00000581378.5:c.629C=
ENST00000582379.1:n.295C=
NM_000018.3:c.911C= NP_000009.1:p.Ala304=
NM_001033859.2:c.845C= NP_001029031.1:p.Ala282=
NM_001270447.1:c.980C= NP_001257376.1:p.Ala327=
NM_001270448.1:c.683C= NP_001257377.1:p.Ala228=
XM_006721516.2:c.911C= XP_006721579.2:p.Ala304=
XM_011523829.1:c.911C= XP_011522131.1:p.Ala304=
XM_011523830.1:c.911C= XP_011522132.1:p.Ala304=
XR_934021.1:n.1018C=
XR_934022.1:n.1018C=
XR_934023.1:n.1018C=
XM_006721516.3:c.911C= XP_006721579.2:p.Ala304=
XM_011523829.2:c.911C= XP_011522131.1:p.Ala304=
XM_011523830.2:c.911C= XP_011522132.1:p.Ala304=
XM_024450741.1:c.911C= XP_024306509.1:p.Ala304=
XR_934021.2:n.970C=
XR_934022.2:n.970C=
XR_934023.2:n.970C=
NM_000018.4:c.911C= MANE Select NP_000009.1:p.Ala304=
NM_001033859.3:c.845C= NP_001029031.1:p.Ala282=
NM_001270447.2:c.980C= NP_001257376.1:p.Ala327=
NM_001270448.2:c.683C= NP_001257377.1:p.Ala228=