Canonical Allele Identifier: CA397723346
Gene: ACADVL HGNC NCBI

Linked Data

dbSNP Id: rs775400380
MyVariant Identifiers: chr17:g.7125276A>G (hg19) chr17:g.7221957A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221957A>G , CM000679.2:g.7221957A>G GRCh38
NC_000017.10:g.7125276A>G , CM000679.1:g.7125276A>G GRCh37
NC_000017.9:g.7066000A>G NCBI36
NG_007975.1:g.7124A>G
NG_008391.2:g.3094T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.628A>G MANE Select ENSP00000349297.5:p.Thr210Ala
ENST00000322910.9:c.*583A>G ENSP00000325395.5:n.*583A>G
ENST00000350303.9:c.562A>G ENSP00000344152.5:p.Thr188Ala
ENST00000356839.9:c.628A>G ENSP00000349297.5:p.Thr210Ala
ENST00000543245.6:c.697A>G ENSP00000438689.2:p.Thr233Ala
ENST00000577191.5:n.705A>G
ENST00000577857.5:n.444A>G
ENST00000579286.5:n.809A>G
ENST00000580365.1:n.359A>G
ENST00000581378.5:c.346A>G
ENST00000581562.5:n.530A>G
ENST00000582379.1:n.12A>G
ENST00000583312.5:c.643A>G ENSP00000467920.1:p.Thr215Ala
ENST00000583760.1:n.410A>G
NM_000018.3:c.628A>G NP_000009.1:p.Thr210Ala
NM_001033859.2:c.562A>G NP_001029031.1:p.Thr188Ala
NM_001270447.1:c.697A>G NP_001257376.1:p.Thr233Ala
NM_001270448.1:c.400A>G NP_001257377.1:p.Thr134Ala
XM_006721516.2:c.628A>G XP_006721579.2:p.Thr210Ala
XM_011523829.1:c.628A>G XP_011522131.1:p.Thr210Ala
XM_011523830.1:c.628A>G XP_011522132.1:p.Thr210Ala
XR_934021.1:n.735A>G
XR_934022.1:n.735A>G
XR_934023.1:n.735A>G
XM_006721516.3:c.628A>G XP_006721579.2:p.Thr210Ala
XM_011523829.2:c.628A>G XP_011522131.1:p.Thr210Ala
XM_011523830.2:c.628A>G XP_011522132.1:p.Thr210Ala
XM_024450741.1:c.628A>G XP_024306509.1:p.Thr210Ala
XR_934021.2:n.687A>G
XR_934022.2:n.687A>G
XR_934023.2:n.687A>G
NM_000018.4:c.628A>G MANE Select NP_000009.1:p.Thr210Ala
NM_001033859.3:c.562A>G NP_001029031.1:p.Thr188Ala
NM_001270447.2:c.697A>G NP_001257376.1:p.Thr233Ala
NM_001270448.2:c.400A>G NP_001257377.1:p.Thr134Ala
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