Canonical Allele Identifier: CA497694170
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7127152A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223833A>G , CM000679.2:g.7223833A>G GRCh38
NC_000017.10:g.7127152A>G , CM000679.1:g.7127152A>G GRCh37
NC_000017.9:g.7067876A>G NCBI36
NG_007975.1:g.9000A>G
NG_008391.2:g.1218T>C
NG_033038.1:g.15712T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1290A>G MANE Select ENSP00000349297.5:p.Thr430=
ENST00000322910.9:c.*1245A>G ENSP00000325395.5:n.*1245A>G
ENST00000350303.9:c.1224A>G ENSP00000344152.5:p.Thr408=
ENST00000356839.9:c.1290A>G ENSP00000349297.5:p.Thr430=
ENST00000542255.6:c.148A>G
ENST00000543245.6:c.1359A>G ENSP00000438689.2:p.Thr453=
ENST00000578711.1:n.329A>G
ENST00000578824.5:n.706A>G
ENST00000579425.5:n.314A>G
ENST00000579546.1:c.127A>G
ENST00000583074.5:n.9A>G
ENST00000583850.5:n.65A>G
ENST00000583858.5:c.319A>G
ENST00000585203.6:n.498A>G
NM_000018.3:c.1290A>G NP_000009.1:p.Thr430=
NM_001033859.2:c.1224A>G NP_001029031.1:p.Thr408=
NM_001270447.1:c.1359A>G NP_001257376.1:p.Thr453=
NM_001270448.1:c.1062A>G NP_001257377.1:p.Thr354=
XM_006721516.2:c.1290A>G XP_006721579.2:p.Thr430=
XM_011523829.1:c.1290A>G XP_011522131.1:p.Thr430=
XM_011523830.1:c.1290A>G XP_011522132.1:p.Thr430=
XR_934021.1:n.1397A>G
XR_934022.1:n.1397A>G
XR_934023.1:n.1397A>G
XM_006721516.3:c.1290A>G XP_006721579.2:p.Thr430=
XM_011523829.2:c.1290A>G XP_011522131.1:p.Thr430=
XM_011523830.2:c.1290A>G XP_011522132.1:p.Thr430=
XM_024450741.1:c.1290A>G XP_024306509.1:p.Thr430=
XR_934021.2:n.1349A>G
XR_934022.2:n.1349A>G
XR_934023.2:n.1349A>G
NM_000018.4:c.1290A>G MANE Select NP_000009.1:p.Thr430=
NM_001033859.3:c.1224A>G NP_001029031.1:p.Thr408=
NM_001270447.2:c.1359A>G NP_001257376.1:p.Thr453=
NM_001270448.2:c.1062A>G NP_001257377.1:p.Thr354=
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