Canonical Allele Identifier: CA397724296
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7126183C>A (hg19) chr17:g.7222864C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222864C>A , CM000679.2:g.7222864C>A GRCh38
NC_000017.10:g.7126183C>A , CM000679.1:g.7126183C>A GRCh37
NC_000017.9:g.7066907C>A NCBI36
NG_007975.1:g.8031C>A
NG_008391.2:g.2187G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1076C>A MANE Select ENSP00000349297.5:p.Ala359Glu
ENST00000322910.9:c.*1031C>A ENSP00000325395.5:n.*1031C>A
ENST00000350303.9:c.1010C>A ENSP00000344152.5:p.Ala337Glu
ENST00000356839.9:c.1076C>A ENSP00000349297.5:p.Ala359Glu
ENST00000543245.6:c.1145C>A ENSP00000438689.2:p.Ala382Glu
ENST00000578824.5:n.225C>A
ENST00000582379.1:n.460C>A
ENST00000583858.5:c.105C>A
ENST00000585203.6:n.17C>A
NM_000018.3:c.1076C>A NP_000009.1:p.Ala359Glu
NM_001033859.2:c.1010C>A NP_001029031.1:p.Ala337Glu
NM_001270447.1:c.1145C>A NP_001257376.1:p.Ala382Glu
NM_001270448.1:c.848C>A NP_001257377.1:p.Ala283Glu
XM_006721516.2:c.1076C>A XP_006721579.2:p.Ala359Glu
XM_011523829.1:c.1076C>A XP_011522131.1:p.Ala359Glu
XM_011523830.1:c.1076C>A XP_011522132.1:p.Ala359Glu
XR_934021.1:n.1183C>A
XR_934022.1:n.1183C>A
XR_934023.1:n.1183C>A
XM_006721516.3:c.1076C>A XP_006721579.2:p.Ala359Glu
XM_011523829.2:c.1076C>A XP_011522131.1:p.Ala359Glu
XM_011523830.2:c.1076C>A XP_011522132.1:p.Ala359Glu
XM_024450741.1:c.1076C>A XP_024306509.1:p.Ala359Glu
XR_934021.2:n.1135C>A
XR_934022.2:n.1135C>A
XR_934023.2:n.1135C>A
NM_000018.4:c.1076C>A MANE Select NP_000009.1:p.Ala359Glu
NM_001033859.3:c.1010C>A NP_001029031.1:p.Ala337Glu
NM_001270447.2:c.1145C>A NP_001257376.1:p.Ala382Glu
NM_001270448.2:c.848C>A NP_001257377.1:p.Ala283Glu
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