Canonical Allele Identifier: CA397722405
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7220641A>G , CM000679.2:g.7220641A>G GRCh38
NC_000017.10:g.7123960A>G , CM000679.1:g.7123960A>G GRCh37
NC_000017.9:g.7064684A>G NCBI36
NG_007975.1:g.5808A>G
NG_008391.2:g.4410T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.242A>G MANE Select ENSP00000349297.5:p.Gln81Arg
ENST00000322910.9:c.*197A>G ENSP00000325395.5:n.*197A>G
ENST00000350303.9:c.176A>G ENSP00000344152.5:p.Gln59Arg
ENST00000356839.9:c.242A>G ENSP00000349297.5:p.Gln81Arg
ENST00000543245.6:c.311A>G ENSP00000438689.2:p.Gln104Arg
ENST00000577191.5:n.319A>G
ENST00000577433.5:n.450A>G
ENST00000577857.5:n.229-125A>G
ENST00000578269.5:n.689A>G
ENST00000578421.1:n.450A>G
ENST00000579286.5:n.423A>G
ENST00000579886.2:c.201+115A>G ENSP00000463246.1:n.201+115A>G
ENST00000580263.5:n.406A>G
ENST00000581562.5:n.289A>G
ENST00000582056.5:n.332A>G
ENST00000582166.1:n.130A>G
ENST00000582356.5:n.441A>G
ENST00000583312.5:c.242A>G ENSP00000467920.1:p.Gln81Arg
ENST00000584103.5:c.242A>G ENSP00000465353.1:p.Gln81Arg
NM_000018.3:c.242A>G NP_000009.1:p.Gln81Arg
NM_001033859.2:c.176A>G NP_001029031.1:p.Gln59Arg
NM_001270447.1:c.311A>G NP_001257376.1:p.Gln104Arg
NM_001270448.1:c.14A>G NP_001257377.1:p.Gln5Arg
XM_006721516.2:c.242A>G XP_006721579.2:p.Gln81Arg
XM_011523829.1:c.242A>G XP_011522131.1:p.Gln81Arg
XM_011523830.1:c.242A>G XP_011522132.1:p.Gln81Arg
XR_934021.1:n.349A>G
XR_934022.1:n.349A>G
XR_934023.1:n.349A>G
XM_006721516.3:c.242A>G XP_006721579.2:p.Gln81Arg
XM_011523829.2:c.242A>G XP_011522131.1:p.Gln81Arg
XM_011523830.2:c.242A>G XP_011522132.1:p.Gln81Arg
XM_024450741.1:c.242A>G XP_024306509.1:p.Gln81Arg
XR_934021.2:n.301A>G
XR_934022.2:n.301A>G
XR_934023.2:n.301A>G
NM_000018.4:c.242A>G MANE Select NP_000009.1:p.Gln81Arg
NM_001033859.3:c.176A>G NP_001029031.1:p.Gln59Arg
NM_001270447.2:c.311A>G NP_001257376.1:p.Gln104Arg
NM_001270448.2:c.14A>G NP_001257377.1:p.Gln5Arg