Canonical Allele Identifier: CA2245709514
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222751C= , CM000679.2:g.7222751C= GRCh38
NC_000017.10:g.7126070C= , CM000679.1:g.7126070C= GRCh37
NC_000017.9:g.7066794C= NCBI36
NG_007975.1:g.7918C=
NG_008391.2:g.2300G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.963C= MANE Select ENSP00000349297.5:p.Asn321=
ENST00000322910.9:c.*918C= ENSP00000325395.5:n.*918C=
ENST00000350303.9:c.897C= ENSP00000344152.5:p.Asn299=
ENST00000356839.9:c.963C= ENSP00000349297.5:p.Asn321=
ENST00000543245.6:c.1032C= ENSP00000438689.2:p.Asn344=
ENST00000578824.5:n.112C=
ENST00000581378.5:c.681C=
ENST00000582379.1:n.347C=
NM_000018.3:c.963C= NP_000009.1:p.Asn321=
NM_001033859.2:c.897C= NP_001029031.1:p.Asn299=
NM_001270447.1:c.1032C= NP_001257376.1:p.Asn344=
NM_001270448.1:c.735C= NP_001257377.1:p.Asn245=
XM_006721516.2:c.963C= XP_006721579.2:p.Asn321=
XM_011523829.1:c.963C= XP_011522131.1:p.Asn321=
XM_011523830.1:c.963C= XP_011522132.1:p.Asn321=
XR_934021.1:n.1070C=
XR_934022.1:n.1070C=
XR_934023.1:n.1070C=
XM_006721516.3:c.963C= XP_006721579.2:p.Asn321=
XM_011523829.2:c.963C= XP_011522131.1:p.Asn321=
XM_011523830.2:c.963C= XP_011522132.1:p.Asn321=
XM_024450741.1:c.963C= XP_024306509.1:p.Asn321=
XR_934021.2:n.1022C=
XR_934022.2:n.1022C=
XR_934023.2:n.1022C=
NM_000018.4:c.963C= MANE Select NP_000009.1:p.Asn321=
NM_001033859.3:c.897C= NP_001029031.1:p.Asn299=
NM_001270447.2:c.1032C= NP_001257376.1:p.Asn344=
NM_001270448.2:c.735C= NP_001257377.1:p.Asn245=