Canonical Allele Identifier: CA397725259
Gene: ACADVL HGNC NCBI

Linked Data

dbSNP Id: rs2071365861

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224213T>C , CM000679.2:g.7224213T>C GRCh38
NC_000017.10:g.7127532T>C , CM000679.1:g.7127532T>C GRCh37
NC_000017.9:g.7068256T>C NCBI36
NG_007975.1:g.9380T>C
NG_008391.2:g.838A>G
NG_033038.1:g.15332A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1502T>C MANE Select ENSP00000349297.5:p.Leu501Pro
ENST00000322910.9:c.*1457T>C ENSP00000325395.5:n.*1457T>C
ENST00000350303.9:c.1436T>C ENSP00000344152.5:p.Leu479Pro
ENST00000356839.9:c.1502T>C ENSP00000349297.5:p.Leu501Pro
ENST00000542255.6:c.360T>C
ENST00000543245.6:c.1571T>C ENSP00000438689.2:p.Leu524Pro
ENST00000578711.1:n.709T>C
ENST00000579391.1:n.110T>C
ENST00000579425.5:n.618T>C
ENST00000579546.1:c.272-108T>C
ENST00000579894.5:n.289T>C
ENST00000583074.5:n.154-108T>C
ENST00000583850.5:n.277T>C
ENST00000583858.5:c.464-108T>C
ENST00000585203.6:n.693T>C
NM_000018.3:c.1502T>C NP_000009.1:p.Leu501Pro
NM_001033859.2:c.1436T>C NP_001029031.1:p.Leu479Pro
NM_001270447.1:c.1571T>C NP_001257376.1:p.Leu524Pro
NM_001270448.1:c.1274T>C NP_001257377.1:p.Leu425Pro
XM_006721516.2:c.1502T>C XP_006721579.2:p.Leu501Pro
XM_011523829.1:c.1435-108T>C XP_011522131.1:n.1435-108T>C
XM_011523830.1:c.1435-108T>C XP_011522132.1:n.1435-108T>C
XR_934021.1:n.1609T>C
XR_934022.1:n.1542-108T>C
XR_934023.1:n.1542-108T>C
XM_006721516.3:c.1502T>C XP_006721579.2:p.Leu501Pro
XM_011523829.2:c.1435-108T>C XP_011522131.1:n.1435-108T>C
XM_011523830.2:c.1435-108T>C XP_011522132.1:n.1435-108T>C
XM_024450741.1:c.1435-108T>C XP_024306509.1:n.1435-108T>C
XR_934021.2:n.1561T>C
XR_934022.2:n.1494-108T>C
XR_934023.2:n.1494-108T>C
NM_000018.4:c.1502T>C MANE Select NP_000009.1:p.Leu501Pro
NM_001033859.3:c.1436T>C NP_001029031.1:p.Leu479Pro
NM_001270447.2:c.1571T>C NP_001257376.1:p.Leu524Pro
NM_001270448.2:c.1274T>C NP_001257377.1:p.Leu425Pro