Canonical Allele Identifier: CA497694230
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7127494C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224175C>T , CM000679.2:g.7224175C>T GRCh38
NC_000017.10:g.7127494C>T , CM000679.1:g.7127494C>T GRCh37
NC_000017.9:g.7068218C>T NCBI36
NG_007975.1:g.9342C>T
NG_008391.2:g.876G>A
NG_033038.1:g.15370G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1464C>T MANE Select ENSP00000349297.5:p.Gly488=
ENST00000322910.9:c.*1419C>T ENSP00000325395.5:n.*1419C>T
ENST00000350303.9:c.1398C>T ENSP00000344152.5:p.Gly466=
ENST00000356839.9:c.1464C>T ENSP00000349297.5:p.Gly488=
ENST00000542255.6:c.322C>T
ENST00000543245.6:c.1533C>T ENSP00000438689.2:p.Gly511=
ENST00000578711.1:n.671C>T
ENST00000579391.1:n.72C>T
ENST00000579425.5:n.580C>T
ENST00000579546.1:c.271+106C>T
ENST00000579894.5:n.251C>T
ENST00000583074.5:n.153+106C>T
ENST00000583850.5:n.239C>T
ENST00000583858.5:c.463+106C>T
ENST00000585203.6:n.655C>T
NM_000018.3:c.1464C>T NP_000009.1:p.Gly488=
NM_001033859.2:c.1398C>T NP_001029031.1:p.Gly466=
NM_001270447.1:c.1533C>T NP_001257376.1:p.Gly511=
NM_001270448.1:c.1236C>T NP_001257377.1:p.Gly412=
XM_006721516.2:c.1464C>T XP_006721579.2:p.Gly488=
XM_011523829.1:c.1434+106C>T XP_011522131.1:n.1434+106C>T
XM_011523830.1:c.1434+106C>T XP_011522132.1:n.1434+106C>T
XR_934021.1:n.1571C>T
XR_934022.1:n.1541+106C>T
XR_934023.1:n.1541+106C>T
XM_006721516.3:c.1464C>T XP_006721579.2:p.Gly488=
XM_011523829.2:c.1434+106C>T XP_011522131.1:n.1434+106C>T
XM_011523830.2:c.1434+106C>T XP_011522132.1:n.1434+106C>T
XM_024450741.1:c.1434+106C>T XP_024306509.1:n.1434+106C>T
XR_934021.2:n.1523C>T
XR_934022.2:n.1493+106C>T
XR_934023.2:n.1493+106C>T
NM_000018.4:c.1464C>T MANE Select NP_000009.1:p.Gly488=
NM_001033859.3:c.1398C>T NP_001029031.1:p.Gly466=
NM_001270447.2:c.1533C>T NP_001257376.1:p.Gly511=
NM_001270448.2:c.1236C>T NP_001257377.1:p.Gly412=
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