Canonical Allele Identifier: CA397724613
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7126994A>T (hg19) chr17:g.7223675A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223675A>T , CM000679.2:g.7223675A>T GRCh38
NC_000017.10:g.7126994A>T , CM000679.1:g.7126994A>T GRCh37
NC_000017.9:g.7067718A>T NCBI36
NG_007975.1:g.8842A>T
NG_008391.2:g.1376T>A
NG_033038.1:g.15870T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1214A>T MANE Select ENSP00000349297.5:p.Asp405Val
ENST00000322910.9:c.*1169A>T ENSP00000325395.5:n.*1169A>T
ENST00000350303.9:c.1148A>T ENSP00000344152.5:p.Asp383Val
ENST00000356839.9:c.1214A>T ENSP00000349297.5:p.Asp405Val
ENST00000542255.6:c.72A>T
ENST00000543245.6:c.1283A>T ENSP00000438689.2:p.Asp428Val
ENST00000578579.2:n.385A>T
ENST00000578711.1:n.171A>T
ENST00000578824.5:n.630A>T
ENST00000579425.5:n.238A>T
ENST00000579546.1:c.51A>T
ENST00000583858.5:c.243A>T
ENST00000585203.6:n.422A>T
NM_000018.3:c.1214A>T NP_000009.1:p.Asp405Val
NM_001033859.2:c.1148A>T NP_001029031.1:p.Asp383Val
NM_001270447.1:c.1283A>T NP_001257376.1:p.Asp428Val
NM_001270448.1:c.986A>T NP_001257377.1:p.Asp329Val
XM_006721516.2:c.1214A>T XP_006721579.2:p.Asp405Val
XM_011523829.1:c.1214A>T XP_011522131.1:p.Asp405Val
XM_011523830.1:c.1214A>T XP_011522132.1:p.Asp405Val
XR_934021.1:n.1321A>T
XR_934022.1:n.1321A>T
XR_934023.1:n.1321A>T
XM_006721516.3:c.1214A>T XP_006721579.2:p.Asp405Val
XM_011523829.2:c.1214A>T XP_011522131.1:p.Asp405Val
XM_011523830.2:c.1214A>T XP_011522132.1:p.Asp405Val
XM_024450741.1:c.1214A>T XP_024306509.1:p.Asp405Val
XR_934021.2:n.1273A>T
XR_934022.2:n.1273A>T
XR_934023.2:n.1273A>T
NM_000018.4:c.1214A>T MANE Select NP_000009.1:p.Asp405Val
NM_001033859.3:c.1148A>T NP_001029031.1:p.Asp383Val
NM_001270447.2:c.1283A>T NP_001257376.1:p.Asp428Val
NM_001270448.2:c.986A>T NP_001257377.1:p.Asp329Val
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