Canonical Allele Identifier: CA397723233
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221653A>G , CM000679.2:g.7221653A>G GRCh38
NC_000017.10:g.7124972A>G , CM000679.1:g.7124972A>G GRCh37
NC_000017.9:g.7065696A>G NCBI36
NG_007975.1:g.6820A>G
NG_008391.2:g.3398T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.593A>G MANE Select ENSP00000349297.5:p.Lys198Arg
ENST00000322910.9:c.*548A>G ENSP00000325395.5:n.*548A>G
ENST00000350303.9:c.527A>G ENSP00000344152.5:p.Lys176Arg
ENST00000356839.9:c.593A>G ENSP00000349297.5:p.Lys198Arg
ENST00000543245.6:c.662A>G ENSP00000438689.2:p.Lys221Arg
ENST00000577191.5:n.670A>G
ENST00000577433.5:n.801A>G
ENST00000577857.5:n.409A>G
ENST00000579286.5:n.774A>G
ENST00000579886.2:c.431A>G ENSP00000463246.1:p.Lys144Arg
ENST00000580365.1:n.324A>G
ENST00000581378.5:c.311A>G
ENST00000581562.5:n.525-299A>G
ENST00000583312.5:c.593A>G ENSP00000467920.1:p.Lys198Arg
ENST00000583760.1:n.375A>G
NM_000018.3:c.593A>G NP_000009.1:p.Lys198Arg
NM_001033859.2:c.527A>G NP_001029031.1:p.Lys176Arg
NM_001270447.1:c.662A>G NP_001257376.1:p.Lys221Arg
NM_001270448.1:c.365A>G NP_001257377.1:p.Lys122Arg
XM_006721516.2:c.593A>G XP_006721579.2:p.Lys198Arg
XM_011523829.1:c.593A>G XP_011522131.1:p.Lys198Arg
XM_011523830.1:c.593A>G XP_011522132.1:p.Lys198Arg
XR_934021.1:n.700A>G
XR_934022.1:n.700A>G
XR_934023.1:n.700A>G
XM_006721516.3:c.593A>G XP_006721579.2:p.Lys198Arg
XM_011523829.2:c.593A>G XP_011522131.1:p.Lys198Arg
XM_011523830.2:c.593A>G XP_011522132.1:p.Lys198Arg
XM_024450741.1:c.593A>G XP_024306509.1:p.Lys198Arg
XR_934021.2:n.652A>G
XR_934022.2:n.652A>G
XR_934023.2:n.652A>G
NM_000018.4:c.593A>G MANE Select NP_000009.1:p.Lys198Arg
NM_001033859.3:c.527A>G NP_001029031.1:p.Lys176Arg
NM_001270447.2:c.662A>G NP_001257376.1:p.Lys221Arg
NM_001270448.2:c.365A>G NP_001257377.1:p.Lys122Arg