Canonical Allele Identifier: CA2245714484
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224505C= , CM000679.2:g.7224505C= GRCh38
NC_000017.10:g.7127824C= , CM000679.1:g.7127824C= GRCh37
NC_000017.9:g.7068548C= NCBI36
NG_007975.1:g.9672C=
NG_008391.2:g.546G=
NG_033038.1:g.15040G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1631C= MANE Select ENSP00000349297.5:p.Ala544=
ENST00000322910.9:c.*1586C= ENSP00000325395.5:n.*1586C=
ENST00000350303.9:c.1565C= ENSP00000344152.5:p.Ala522=
ENST00000356839.9:c.1631C= ENSP00000349297.5:p.Ala544=
ENST00000542255.6:c.489C=
ENST00000543245.6:c.1700C= ENSP00000438689.2:p.Ala567=
ENST00000578319.5:n.212C=
ENST00000578711.1:n.1001C=
ENST00000578809.5:n.203C=
ENST00000579391.1:n.235C=
ENST00000579425.5:n.747C=
ENST00000579546.1:c.366C=
ENST00000579894.5:n.418C=
ENST00000582450.1:n.139C=
ENST00000583074.5:n.252C=
ENST00000583848.5:c.17C= ENSP00000466487.1:p.Ala6=
ENST00000583850.5:n.402C=
ENST00000583858.5:c.562C=
ENST00000585203.6:n.822C=
NM_000018.3:c.1631C= NP_000009.1:p.Ala544=
NM_001033859.2:c.1565C= NP_001029031.1:p.Ala522=
NM_001270447.1:c.1700C= NP_001257376.1:p.Ala567=
NM_001270448.1:c.1403C= NP_001257377.1:p.Ala468=
XM_006721516.2:c.1631C= XP_006721579.2:p.Ala544=
XM_011523829.1:c.1529C= XP_011522131.1:p.Ala510=
XM_011523830.1:c.1529C= XP_011522132.1:p.Ala510=
XR_934021.1:n.1734C=
XR_934022.1:n.1640C=
XR_934023.1:n.1640C=
XM_006721516.3:c.1631C= XP_006721579.2:p.Ala544=
XM_011523829.2:c.1529C= XP_011522131.1:p.Ala510=
XM_011523830.2:c.1529C= XP_011522132.1:p.Ala510=
XM_024450741.1:c.1619C= XP_024306509.1:p.Ala540=
XR_934021.2:n.1686C=
XR_934022.2:n.1592C=
XR_934023.2:n.1592C=
NM_000018.4:c.1631C= MANE Select NP_000009.1:p.Ala544=
NM_001033859.3:c.1565C= NP_001029031.1:p.Ala522=
NM_001270447.2:c.1700C= NP_001257376.1:p.Ala567=
NM_001270448.2:c.1403C= NP_001257377.1:p.Ala468=