Canonical Allele Identifier: CA497694024
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7125338C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222019C>G , CM000679.2:g.7222019C>G GRCh38
NC_000017.10:g.7125338C>G , CM000679.1:g.7125338C>G GRCh37
NC_000017.9:g.7066062C>G NCBI36
NG_007975.1:g.7186C>G
NG_008391.2:g.3032G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.690C>G MANE Select ENSP00000349297.5:p.Thr230=
ENST00000322910.9:c.*645C>G ENSP00000325395.5:n.*645C>G
ENST00000350303.9:c.624C>G ENSP00000344152.5:p.Thr208=
ENST00000356839.9:c.690C>G ENSP00000349297.5:p.Thr230=
ENST00000543245.6:c.759C>G ENSP00000438689.2:p.Thr253=
ENST00000577191.5:n.767C>G
ENST00000577857.5:n.506C>G
ENST00000579286.5:n.871C>G
ENST00000580365.1:n.421C>G
ENST00000581378.5:c.408C>G
ENST00000582379.1:n.74C>G
ENST00000583760.1:n.472C>G
NM_000018.3:c.690C>G NP_000009.1:p.Thr230=
NM_001033859.2:c.624C>G NP_001029031.1:p.Thr208=
NM_001270447.1:c.759C>G NP_001257376.1:p.Thr253=
NM_001270448.1:c.462C>G NP_001257377.1:p.Thr154=
XM_006721516.2:c.690C>G XP_006721579.2:p.Thr230=
XM_011523829.1:c.690C>G XP_011522131.1:p.Thr230=
XM_011523830.1:c.690C>G XP_011522132.1:p.Thr230=
XR_934021.1:n.797C>G
XR_934022.1:n.797C>G
XR_934023.1:n.797C>G
XM_006721516.3:c.690C>G XP_006721579.2:p.Thr230=
XM_011523829.2:c.690C>G XP_011522131.1:p.Thr230=
XM_011523830.2:c.690C>G XP_011522132.1:p.Thr230=
XM_024450741.1:c.690C>G XP_024306509.1:p.Thr230=
XR_934021.2:n.749C>G
XR_934022.2:n.749C>G
XR_934023.2:n.749C>G
NM_000018.4:c.690C>G MANE Select NP_000009.1:p.Thr230=
NM_001033859.3:c.624C>G NP_001029031.1:p.Thr208=
NM_001270447.2:c.759C>G NP_001257376.1:p.Thr253=
NM_001270448.2:c.462C>G NP_001257377.1:p.Thr154=
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