Canonical Allele Identifier: CA397723463
Gene: ACADVL HGNC NCBI

Linked Data

ClinVar Variation Id: 1369864
ClinVar RCV Id: RCV001870855
dbSNP Id: rs786204536
MyVariant Identifiers: chr17:g.7125333C>G (hg19) chr17:g.7222014C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222014C>G , CM000679.2:g.7222014C>G GRCh38
NC_000017.10:g.7125333C>G , CM000679.1:g.7125333C>G GRCh37
NC_000017.9:g.7066057C>G NCBI36
NG_007975.1:g.7181C>G
NG_008391.2:g.3037G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.685C>G MANE Select ENSP00000349297.5:p.Arg229Gly
ENST00000322910.9:c.*640C>G ENSP00000325395.5:n.*640C>G
ENST00000350303.9:c.619C>G ENSP00000344152.5:p.Arg207Gly
ENST00000356839.9:c.685C>G ENSP00000349297.5:p.Arg229Gly
ENST00000543245.6:c.754C>G ENSP00000438689.2:p.Arg252Gly
ENST00000577191.5:n.762C>G
ENST00000577857.5:n.501C>G
ENST00000579286.5:n.866C>G
ENST00000580365.1:n.416C>G
ENST00000581378.5:c.403C>G
ENST00000582379.1:n.69C>G
ENST00000583760.1:n.467C>G
NM_000018.3:c.685C>G NP_000009.1:p.Arg229Gly
NM_001033859.2:c.619C>G NP_001029031.1:p.Arg207Gly
NM_001270447.1:c.754C>G NP_001257376.1:p.Arg252Gly
NM_001270448.1:c.457C>G NP_001257377.1:p.Arg153Gly
XM_006721516.2:c.685C>G XP_006721579.2:p.Arg229Gly
XM_011523829.1:c.685C>G XP_011522131.1:p.Arg229Gly
XM_011523830.1:c.685C>G XP_011522132.1:p.Arg229Gly
XR_934021.1:n.792C>G
XR_934022.1:n.792C>G
XR_934023.1:n.792C>G
XM_006721516.3:c.685C>G XP_006721579.2:p.Arg229Gly
XM_011523829.2:c.685C>G XP_011522131.1:p.Arg229Gly
XM_011523830.2:c.685C>G XP_011522132.1:p.Arg229Gly
XM_024450741.1:c.685C>G XP_024306509.1:p.Arg229Gly
XR_934021.2:n.744C>G
XR_934022.2:n.744C>G
XR_934023.2:n.744C>G
NM_000018.4:c.685C>G MANE Select NP_000009.1:p.Arg229Gly
NM_001033859.3:c.619C>G NP_001029031.1:p.Arg207Gly
NM_001270447.2:c.754C>G NP_001257376.1:p.Arg252Gly
NM_001270448.2:c.457C>G NP_001257377.1:p.Arg153Gly
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