Canonical Allele Identifier: CA397722588
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7220811C>G , CM000679.2:g.7220811C>G GRCh38
NC_000017.10:g.7124130C>G , CM000679.1:g.7124130C>G GRCh37
NC_000017.9:g.7064854C>G NCBI36
NG_007975.1:g.5978C>G
NG_008391.2:g.4240G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000356839.10:c.323C>G MANE Select ENSP00000349297.5:p.Pro108Arg
ENST00000322910.9:c.*278C>G ENSP00000325395.5:n.*278C>G
ENST00000350303.9:c.257C>G ENSP00000344152.5:p.Pro86Arg
ENST00000356839.9:c.323C>G ENSP00000349297.5:p.Pro108Arg
ENST00000543245.6:c.392C>G ENSP00000438689.2:p.Pro131Arg
ENST00000577191.5:n.400C>G
ENST00000577433.5:n.531C>G
ENST00000577857.5:n.274C>G
ENST00000579286.5:n.504C>G
ENST00000579886.2:c.202-134C>G ENSP00000463246.1:n.202-134C>G
ENST00000580365.1:n.54C>G
ENST00000581378.5:c.22C>G
ENST00000581562.5:n.370C>G
ENST00000582056.5:n.413C>G
ENST00000582166.1:n.211C>G
ENST00000582356.5:n.522C>G
ENST00000583312.5:c.323C>G ENSP00000467920.1:p.Pro108Arg
ENST00000584103.5:c.323C>G ENSP00000465353.1:p.Pro108Arg
NM_000018.3:c.323C>G NP_000009.1:p.Pro108Arg
NM_001033859.2:c.257C>G NP_001029031.1:p.Pro86Arg
NM_001270447.1:c.392C>G NP_001257376.1:p.Pro131Arg
NM_001270448.1:c.95C>G NP_001257377.1:p.Pro32Arg
XM_006721516.2:c.323C>G XP_006721579.2:p.Pro108Arg
XM_011523829.1:c.323C>G XP_011522131.1:p.Pro108Arg
XM_011523830.1:c.323C>G XP_011522132.1:p.Pro108Arg
XR_934021.1:n.430C>G
XR_934022.1:n.430C>G
XR_934023.1:n.430C>G
XM_006721516.3:c.323C>G XP_006721579.2:p.Pro108Arg
XM_011523829.2:c.323C>G XP_011522131.1:p.Pro108Arg
XM_011523830.2:c.323C>G XP_011522132.1:p.Pro108Arg
XM_024450741.1:c.323C>G XP_024306509.1:p.Pro108Arg
XR_934021.2:n.382C>G
XR_934022.2:n.382C>G
XR_934023.2:n.382C>G
NM_000018.4:c.323C>G MANE Select NP_000009.1:p.Pro108Arg
NM_001033859.3:c.257C>G NP_001029031.1:p.Pro86Arg
NM_001270447.2:c.392C>G NP_001257376.1:p.Pro131Arg
NM_001270448.2:c.95C>G NP_001257377.1:p.Pro32Arg