Canonical Allele Identifier: CA397725260
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7127532T>G (hg19) chr17:g.7224213T>G (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1502T>G MANE Select ENSP00000349297.5:p.Leu501Arg
ENST00000322910.9:c.*1457T>G ENSP00000325395.5:n.*1457T>G
ENST00000350303.9:c.1436T>G ENSP00000344152.5:p.Leu479Arg
ENST00000356839.9:c.1502T>G ENSP00000349297.5:p.Leu501Arg
ENST00000542255.6:c.360T>G
ENST00000543245.6:c.1571T>G ENSP00000438689.2:p.Leu524Arg
ENST00000578711.1:n.709T>G
ENST00000579391.1:n.110T>G
ENST00000579425.5:n.618T>G
ENST00000579546.1:c.272-108T>G
ENST00000579894.5:n.289T>G
ENST00000583074.5:n.154-108T>G
ENST00000583850.5:n.277T>G
ENST00000583858.5:c.464-108T>G
ENST00000585203.6:n.693T>G
NM_000018.3:c.1502T>G NP_000009.1:p.Leu501Arg
NM_001033859.2:c.1436T>G NP_001029031.1:p.Leu479Arg
NM_001270447.1:c.1571T>G NP_001257376.1:p.Leu524Arg
NM_001270448.1:c.1274T>G NP_001257377.1:p.Leu425Arg
XM_006721516.2:c.1502T>G XP_006721579.2:p.Leu501Arg
XM_011523829.1:c.1435-108T>G XP_011522131.1:n.1435-108T>G
XM_011523830.1:c.1435-108T>G XP_011522132.1:n.1435-108T>G
XR_934021.1:n.1609T>G
XR_934022.1:n.1542-108T>G
XR_934023.1:n.1542-108T>G
XM_006721516.3:c.1502T>G XP_006721579.2:p.Leu501Arg
XM_011523829.2:c.1435-108T>G XP_011522131.1:n.1435-108T>G
XM_011523830.2:c.1435-108T>G XP_011522132.1:n.1435-108T>G
XM_024450741.1:c.1435-108T>G XP_024306509.1:n.1435-108T>G
XR_934021.2:n.1561T>G
XR_934022.2:n.1494-108T>G
XR_934023.2:n.1494-108T>G
NM_000018.4:c.1502T>G MANE Select NP_000009.1:p.Leu501Arg
NM_001033859.3:c.1436T>G NP_001029031.1:p.Leu479Arg
NM_001270447.2:c.1571T>G NP_001257376.1:p.Leu524Arg
NM_001270448.2:c.1274T>G NP_001257377.1:p.Leu425Arg
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