Canonical Allele Identifier: CA397722610
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7220824C>G , CM000679.2:g.7220824C>G GRCh38
NC_000017.10:g.7124143C>G , CM000679.1:g.7124143C>G GRCh37
NC_000017.9:g.7064867C>G NCBI36
NG_007975.1:g.5991C>G
NG_008391.2:g.4227G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.336C>G MANE Select ENSP00000349297.5:p.Phe112Leu
ENST00000322910.9:c.*291C>G ENSP00000325395.5:n.*291C>G
ENST00000350303.9:c.270C>G ENSP00000344152.5:p.Phe90Leu
ENST00000356839.9:c.336C>G ENSP00000349297.5:p.Phe112Leu
ENST00000543245.6:c.405C>G ENSP00000438689.2:p.Phe135Leu
ENST00000577191.5:n.413C>G
ENST00000577433.5:n.544C>G
ENST00000577857.5:n.287C>G
ENST00000579286.5:n.517C>G
ENST00000579886.2:c.202-121C>G ENSP00000463246.1:n.202-121C>G
ENST00000580365.1:n.67C>G
ENST00000581378.5:c.35C>G
ENST00000581562.5:n.383C>G
ENST00000582056.5:n.426C>G
ENST00000582166.1:n.224C>G
ENST00000582356.5:n.535C>G
ENST00000583312.5:c.336C>G ENSP00000467920.1:p.Phe112Leu
ENST00000584103.5:c.336C>G ENSP00000465353.1:p.Phe112Leu
NM_000018.3:c.336C>G NP_000009.1:p.Phe112Leu
NM_001033859.2:c.270C>G NP_001029031.1:p.Phe90Leu
NM_001270447.1:c.405C>G NP_001257376.1:p.Phe135Leu
NM_001270448.1:c.108C>G NP_001257377.1:p.Phe36Leu
XM_006721516.2:c.336C>G XP_006721579.2:p.Phe112Leu
XM_011523829.1:c.336C>G XP_011522131.1:p.Phe112Leu
XM_011523830.1:c.336C>G XP_011522132.1:p.Phe112Leu
XR_934021.1:n.443C>G
XR_934022.1:n.443C>G
XR_934023.1:n.443C>G
XM_006721516.3:c.336C>G XP_006721579.2:p.Phe112Leu
XM_011523829.2:c.336C>G XP_011522131.1:p.Phe112Leu
XM_011523830.2:c.336C>G XP_011522132.1:p.Phe112Leu
XM_024450741.1:c.336C>G XP_024306509.1:p.Phe112Leu
XR_934021.2:n.395C>G
XR_934022.2:n.395C>G
XR_934023.2:n.395C>G
NM_000018.4:c.336C>G MANE Select NP_000009.1:p.Phe112Leu
NM_001033859.3:c.270C>G NP_001029031.1:p.Phe90Leu
NM_001270447.2:c.405C>G NP_001257376.1:p.Phe135Leu
NM_001270448.2:c.108C>G NP_001257377.1:p.Phe36Leu