Canonical Allele Identifier: CA497619978
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7125586T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222267T>G , CM000679.2:g.7222267T>G GRCh38
NC_000017.10:g.7125586T>G , CM000679.1:g.7125586T>G GRCh37
NC_000017.9:g.7066310T>G NCBI36
NG_007975.1:g.7434T>G
NG_008391.2:g.2784A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.843T>G MANE Select ENSP00000349297.5:p.Ala281=
ENST00000322910.9:c.*798T>G ENSP00000325395.5:n.*798T>G
ENST00000350303.9:c.777T>G ENSP00000344152.5:p.Ala259=
ENST00000356839.9:c.843T>G ENSP00000349297.5:p.Ala281=
ENST00000543245.6:c.912T>G ENSP00000438689.2:p.Ala304=
ENST00000577191.5:n.1015T>G
ENST00000581378.5:c.561T>G
ENST00000582379.1:n.227T>G
NM_000018.3:c.843T>G NP_000009.1:p.Ala281=
NM_001033859.2:c.777T>G NP_001029031.1:p.Ala259=
NM_001270447.1:c.912T>G NP_001257376.1:p.Ala304=
NM_001270448.1:c.615T>G NP_001257377.1:p.Ala205=
XM_006721516.2:c.843T>G XP_006721579.2:p.Ala281=
XM_011523829.1:c.843T>G XP_011522131.1:p.Ala281=
XM_011523830.1:c.843T>G XP_011522132.1:p.Ala281=
XR_934021.1:n.950T>G
XR_934022.1:n.950T>G
XR_934023.1:n.950T>G
XM_006721516.3:c.843T>G XP_006721579.2:p.Ala281=
XM_011523829.2:c.843T>G XP_011522131.1:p.Ala281=
XM_011523830.2:c.843T>G XP_011522132.1:p.Ala281=
XM_024450741.1:c.843T>G XP_024306509.1:p.Ala281=
XR_934021.2:n.902T>G
XR_934022.2:n.902T>G
XR_934023.2:n.902T>G
NM_000018.4:c.843T>G MANE Select NP_000009.1:p.Ala281=
NM_001033859.3:c.777T>G NP_001029031.1:p.Ala259=
NM_001270447.2:c.912T>G NP_001257376.1:p.Ala304=
NM_001270448.2:c.615T>G NP_001257377.1:p.Ala205=
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