Canonical Allele Identifier: CA287436451
Gene: ACADVL HGNC NCBI

Linked Data

dbSNP Id: rs530082418
gnomAD v3: 17-7221653-A-C
gnomAD v4: 17-7221653-A-C

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.593A>C MANE Select ENSP00000349297.5:p.Lys198Thr
ENST00000322910.9:c.*548A>C ENSP00000325395.5:n.*548A>C
ENST00000350303.9:c.527A>C ENSP00000344152.5:p.Lys176Thr
ENST00000356839.9:c.593A>C ENSP00000349297.5:p.Lys198Thr
ENST00000543245.6:c.662A>C ENSP00000438689.2:p.Lys221Thr
ENST00000577191.5:n.670A>C
ENST00000577433.5:n.801A>C
ENST00000577857.5:n.409A>C
ENST00000579286.5:n.774A>C
ENST00000579886.2:c.431A>C ENSP00000463246.1:p.Lys144Thr
ENST00000580365.1:n.324A>C
ENST00000581378.5:c.311A>C
ENST00000581562.5:n.525-299A>C
ENST00000583312.5:c.593A>C ENSP00000467920.1:p.Lys198Thr
ENST00000583760.1:n.375A>C
NM_000018.3:c.593A>C NP_000009.1:p.Lys198Thr
NM_001033859.2:c.527A>C NP_001029031.1:p.Lys176Thr
NM_001270447.1:c.662A>C NP_001257376.1:p.Lys221Thr
NM_001270448.1:c.365A>C NP_001257377.1:p.Lys122Thr
XM_006721516.2:c.593A>C XP_006721579.2:p.Lys198Thr
XM_011523829.1:c.593A>C XP_011522131.1:p.Lys198Thr
XM_011523830.1:c.593A>C XP_011522132.1:p.Lys198Thr
XR_934021.1:n.700A>C
XR_934022.1:n.700A>C
XR_934023.1:n.700A>C
XM_006721516.3:c.593A>C XP_006721579.2:p.Lys198Thr
XM_011523829.2:c.593A>C XP_011522131.1:p.Lys198Thr
XM_011523830.2:c.593A>C XP_011522132.1:p.Lys198Thr
XM_024450741.1:c.593A>C XP_024306509.1:p.Lys198Thr
XR_934021.2:n.652A>C
XR_934022.2:n.652A>C
XR_934023.2:n.652A>C
NM_000018.4:c.593A>C MANE Select NP_000009.1:p.Lys198Thr
NM_001033859.3:c.527A>C NP_001029031.1:p.Lys176Thr
NM_001270447.2:c.662A>C NP_001257376.1:p.Lys221Thr
NM_001270448.2:c.365A>C NP_001257377.1:p.Lys122Thr