Canonical Allele Identifier: CA397723492
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7125349C>A (hg19) chr17:g.7222030C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222030C>A , CM000679.2:g.7222030C>A GRCh38
NC_000017.10:g.7125349C>A , CM000679.1:g.7125349C>A GRCh37
NC_000017.9:g.7066073C>A NCBI36
NG_007975.1:g.7197C>A
NG_008391.2:g.3021G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.701C>A MANE Select ENSP00000349297.5:p.Pro234His
ENST00000322910.9:c.*656C>A ENSP00000325395.5:n.*656C>A
ENST00000350303.9:c.635C>A ENSP00000344152.5:p.Pro212His
ENST00000356839.9:c.701C>A ENSP00000349297.5:p.Pro234His
ENST00000543245.6:c.770C>A ENSP00000438689.2:p.Pro257His
ENST00000577191.5:n.778C>A
ENST00000577857.5:n.517C>A
ENST00000579286.5:n.882C>A
ENST00000580365.1:n.432C>A
ENST00000581378.5:c.419C>A
ENST00000582379.1:n.85C>A
ENST00000583760.1:n.483C>A
NM_000018.3:c.701C>A NP_000009.1:p.Pro234His
NM_001033859.2:c.635C>A NP_001029031.1:p.Pro212His
NM_001270447.1:c.770C>A NP_001257376.1:p.Pro257His
NM_001270448.1:c.473C>A NP_001257377.1:p.Pro158His
XM_006721516.2:c.701C>A XP_006721579.2:p.Pro234His
XM_011523829.1:c.701C>A XP_011522131.1:p.Pro234His
XM_011523830.1:c.701C>A XP_011522132.1:p.Pro234His
XR_934021.1:n.808C>A
XR_934022.1:n.808C>A
XR_934023.1:n.808C>A
XM_006721516.3:c.701C>A XP_006721579.2:p.Pro234His
XM_011523829.2:c.701C>A XP_011522131.1:p.Pro234His
XM_011523830.2:c.701C>A XP_011522132.1:p.Pro234His
XM_024450741.1:c.701C>A XP_024306509.1:p.Pro234His
XR_934021.2:n.760C>A
XR_934022.2:n.760C>A
XR_934023.2:n.760C>A
NM_000018.4:c.701C>A MANE Select NP_000009.1:p.Pro234His
NM_001033859.3:c.635C>A NP_001029031.1:p.Pro212His
NM_001270447.2:c.770C>A NP_001257376.1:p.Pro257His
NM_001270448.2:c.473C>A NP_001257377.1:p.Pro158His
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