Canonical Allele Identifier: CA397723473
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7125339T>C (hg19) chr17:g.7222020T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222020T>C , CM000679.2:g.7222020T>C GRCh38
NC_000017.10:g.7125339T>C , CM000679.1:g.7125339T>C GRCh37
NC_000017.9:g.7066063T>C NCBI36
NG_007975.1:g.7187T>C
NG_008391.2:g.3031A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.691T>C MANE Select ENSP00000349297.5:p.Ser231Pro
ENST00000322910.9:c.*646T>C ENSP00000325395.5:n.*646T>C
ENST00000350303.9:c.625T>C ENSP00000344152.5:p.Ser209Pro
ENST00000356839.9:c.691T>C ENSP00000349297.5:p.Ser231Pro
ENST00000543245.6:c.760T>C ENSP00000438689.2:p.Ser254Pro
ENST00000577191.5:n.768T>C
ENST00000577857.5:n.507T>C
ENST00000579286.5:n.872T>C
ENST00000580365.1:n.422T>C
ENST00000581378.5:c.409T>C
ENST00000582379.1:n.75T>C
ENST00000583760.1:n.473T>C
NM_000018.3:c.691T>C NP_000009.1:p.Ser231Pro
NM_001033859.2:c.625T>C NP_001029031.1:p.Ser209Pro
NM_001270447.1:c.760T>C NP_001257376.1:p.Ser254Pro
NM_001270448.1:c.463T>C NP_001257377.1:p.Ser155Pro
XM_006721516.2:c.691T>C XP_006721579.2:p.Ser231Pro
XM_011523829.1:c.691T>C XP_011522131.1:p.Ser231Pro
XM_011523830.1:c.691T>C XP_011522132.1:p.Ser231Pro
XR_934021.1:n.798T>C
XR_934022.1:n.798T>C
XR_934023.1:n.798T>C
XM_006721516.3:c.691T>C XP_006721579.2:p.Ser231Pro
XM_011523829.2:c.691T>C XP_011522131.1:p.Ser231Pro
XM_011523830.2:c.691T>C XP_011522132.1:p.Ser231Pro
XM_024450741.1:c.691T>C XP_024306509.1:p.Ser231Pro
XR_934021.2:n.750T>C
XR_934022.2:n.750T>C
XR_934023.2:n.750T>C
NM_000018.4:c.691T>C MANE Select NP_000009.1:p.Ser231Pro
NM_001033859.3:c.625T>C NP_001029031.1:p.Ser209Pro
NM_001270447.2:c.760T>C NP_001257376.1:p.Ser254Pro
NM_001270448.2:c.463T>C NP_001257377.1:p.Ser155Pro
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