Canonical Allele Identifier: CA397724867
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7127186T>G (hg19) chr17:g.7223867T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223867T>G , CM000679.2:g.7223867T>G GRCh38
NC_000017.10:g.7127186T>G , CM000679.1:g.7127186T>G GRCh37
NC_000017.9:g.7067910T>G NCBI36
NG_007975.1:g.9034T>G
NG_008391.2:g.1184A>C
NG_033038.1:g.15678A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1324T>G MANE Select ENSP00000349297.5:p.Phe442Val
ENST00000322910.9:c.*1279T>G ENSP00000325395.5:n.*1279T>G
ENST00000350303.9:c.1258T>G ENSP00000344152.5:p.Phe420Val
ENST00000356839.9:c.1324T>G ENSP00000349297.5:p.Phe442Val
ENST00000542255.6:c.182T>G
ENST00000543245.6:c.1393T>G ENSP00000438689.2:p.Phe465Val
ENST00000578711.1:n.363T>G
ENST00000579425.5:n.348T>G
ENST00000579546.1:c.161T>G
ENST00000583074.5:n.43T>G
ENST00000583850.5:n.99T>G
ENST00000583858.5:c.353T>G
ENST00000585203.6:n.523+9T>G
NM_000018.3:c.1324T>G NP_000009.1:p.Phe442Val
NM_001033859.2:c.1258T>G NP_001029031.1:p.Phe420Val
NM_001270447.1:c.1393T>G NP_001257376.1:p.Phe465Val
NM_001270448.1:c.1096T>G NP_001257377.1:p.Phe366Val
XM_006721516.2:c.1324T>G XP_006721579.2:p.Phe442Val
XM_011523829.1:c.1324T>G XP_011522131.1:p.Phe442Val
XM_011523830.1:c.1324T>G XP_011522132.1:p.Phe442Val
XR_934021.1:n.1431T>G
XR_934022.1:n.1431T>G
XR_934023.1:n.1431T>G
XM_006721516.3:c.1324T>G XP_006721579.2:p.Phe442Val
XM_011523829.2:c.1324T>G XP_011522131.1:p.Phe442Val
XM_011523830.2:c.1324T>G XP_011522132.1:p.Phe442Val
XM_024450741.1:c.1324T>G XP_024306509.1:p.Phe442Val
XR_934021.2:n.1383T>G
XR_934022.2:n.1383T>G
XR_934023.2:n.1383T>G
NM_000018.4:c.1324T>G MANE Select NP_000009.1:p.Phe442Val
NM_001033859.3:c.1258T>G NP_001029031.1:p.Phe420Val
NM_001270447.2:c.1393T>G NP_001257376.1:p.Phe465Val
NM_001270448.2:c.1096T>G NP_001257377.1:p.Phe366Val
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