Canonical Allele Identifier: CA397723410
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221988C>T , CM000679.2:g.7221988C>T GRCh38
NC_000017.10:g.7125307C>T , CM000679.1:g.7125307C>T GRCh37
NC_000017.9:g.7066031C>T NCBI36
NG_007975.1:g.7155C>T
NG_008391.2:g.3063G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000356839.10:c.659C>T MANE Select ENSP00000349297.5:p.Ser220Leu
ENST00000322910.9:c.*614C>T ENSP00000325395.5:n.*614C>T
ENST00000350303.9:c.593C>T ENSP00000344152.5:p.Ser198Leu
ENST00000356839.9:c.659C>T ENSP00000349297.5:p.Ser220Leu
ENST00000543245.6:c.728C>T ENSP00000438689.2:p.Ser243Leu
ENST00000577191.5:n.736C>T
ENST00000577857.5:n.475C>T
ENST00000579286.5:n.840C>T
ENST00000580365.1:n.390C>T
ENST00000581378.5:c.377C>T
ENST00000581562.5:n.561C>T
ENST00000582379.1:n.43C>T
ENST00000583312.5:c.674C>T
ENST00000583760.1:n.441C>T
NM_000018.3:c.659C>T NP_000009.1:p.Ser220Leu
NM_001033859.2:c.593C>T NP_001029031.1:p.Ser198Leu
NM_001270447.1:c.728C>T NP_001257376.1:p.Ser243Leu
NM_001270448.1:c.431C>T NP_001257377.1:p.Ser144Leu
XM_006721516.2:c.659C>T XP_006721579.2:p.Ser220Leu
XM_011523829.1:c.659C>T XP_011522131.1:p.Ser220Leu
XM_011523830.1:c.659C>T XP_011522132.1:p.Ser220Leu
XR_934021.1:n.766C>T
XR_934022.1:n.766C>T
XR_934023.1:n.766C>T
XM_006721516.3:c.659C>T XP_006721579.2:p.Ser220Leu
XM_011523829.2:c.659C>T XP_011522131.1:p.Ser220Leu
XM_011523830.2:c.659C>T XP_011522132.1:p.Ser220Leu
XM_024450741.1:c.659C>T XP_024306509.1:p.Ser220Leu
XR_934021.2:n.718C>T
XR_934022.2:n.718C>T
XR_934023.2:n.718C>T
NM_000018.4:c.659C>T MANE Select NP_000009.1:p.Ser220Leu
NM_001033859.3:c.593C>T NP_001029031.1:p.Ser198Leu
NM_001270447.2:c.728C>T NP_001257376.1:p.Ser243Leu
NM_001270448.2:c.431C>T NP_001257377.1:p.Ser144Leu