Canonical Allele Identifier: CA497694027
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7125344T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222025T>A , CM000679.2:g.7222025T>A GRCh38
NC_000017.10:g.7125344T>A , CM000679.1:g.7125344T>A GRCh37
NC_000017.9:g.7066068T>A NCBI36
NG_007975.1:g.7192T>A
NG_008391.2:g.3026A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.696T>A MANE Select ENSP00000349297.5:p.Ala232=
ENST00000322910.9:c.*651T>A ENSP00000325395.5:n.*651T>A
ENST00000350303.9:c.630T>A ENSP00000344152.5:p.Ala210=
ENST00000356839.9:c.696T>A ENSP00000349297.5:p.Ala232=
ENST00000543245.6:c.765T>A ENSP00000438689.2:p.Ala255=
ENST00000577191.5:n.773T>A
ENST00000577857.5:n.512T>A
ENST00000579286.5:n.877T>A
ENST00000580365.1:n.427T>A
ENST00000581378.5:c.414T>A
ENST00000582379.1:n.80T>A
ENST00000583760.1:n.478T>A
NM_000018.3:c.696T>A NP_000009.1:p.Ala232=
NM_001033859.2:c.630T>A NP_001029031.1:p.Ala210=
NM_001270447.1:c.765T>A NP_001257376.1:p.Ala255=
NM_001270448.1:c.468T>A NP_001257377.1:p.Ala156=
XM_006721516.2:c.696T>A XP_006721579.2:p.Ala232=
XM_011523829.1:c.696T>A XP_011522131.1:p.Ala232=
XM_011523830.1:c.696T>A XP_011522132.1:p.Ala232=
XR_934021.1:n.803T>A
XR_934022.1:n.803T>A
XR_934023.1:n.803T>A
XM_006721516.3:c.696T>A XP_006721579.2:p.Ala232=
XM_011523829.2:c.696T>A XP_011522131.1:p.Ala232=
XM_011523830.2:c.696T>A XP_011522132.1:p.Ala232=
XM_024450741.1:c.696T>A XP_024306509.1:p.Ala232=
XR_934021.2:n.755T>A
XR_934022.2:n.755T>A
XR_934023.2:n.755T>A
NM_000018.4:c.696T>A MANE Select NP_000009.1:p.Ala232=
NM_001033859.3:c.630T>A NP_001029031.1:p.Ala210=
NM_001270447.2:c.765T>A NP_001257376.1:p.Ala255=
NM_001270448.2:c.468T>A NP_001257377.1:p.Ala156=
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