Canonical Allele Identifier: CA397724717
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7127042T>A (hg19) chr17:g.7223723T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223723T>A , CM000679.2:g.7223723T>A GRCh38
NC_000017.10:g.7127042T>A , CM000679.1:g.7127042T>A GRCh37
NC_000017.9:g.7067766T>A NCBI36
NG_007975.1:g.8890T>A
NG_008391.2:g.1328A>T
NG_033038.1:g.15822A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1262T>A MANE Select ENSP00000349297.5:p.Phe421Tyr
ENST00000322910.9:c.*1217T>A ENSP00000325395.5:n.*1217T>A
ENST00000350303.9:c.1196T>A ENSP00000344152.5:p.Phe399Tyr
ENST00000356839.9:c.1262T>A ENSP00000349297.5:p.Phe421Tyr
ENST00000542255.6:c.120T>A
ENST00000543245.6:c.1331T>A ENSP00000438689.2:p.Phe444Tyr
ENST00000578579.2:n.433T>A
ENST00000578711.1:n.219T>A
ENST00000578824.5:n.678T>A
ENST00000579425.5:n.286T>A
ENST00000579546.1:c.99T>A
ENST00000583850.5:n.37T>A
ENST00000583858.5:c.291T>A
ENST00000585203.6:n.470T>A
NM_000018.3:c.1262T>A NP_000009.1:p.Phe421Tyr
NM_001033859.2:c.1196T>A NP_001029031.1:p.Phe399Tyr
NM_001270447.1:c.1331T>A NP_001257376.1:p.Phe444Tyr
NM_001270448.1:c.1034T>A NP_001257377.1:p.Phe345Tyr
XM_006721516.2:c.1262T>A XP_006721579.2:p.Phe421Tyr
XM_011523829.1:c.1262T>A XP_011522131.1:p.Phe421Tyr
XM_011523830.1:c.1262T>A XP_011522132.1:p.Phe421Tyr
XR_934021.1:n.1369T>A
XR_934022.1:n.1369T>A
XR_934023.1:n.1369T>A
XM_006721516.3:c.1262T>A XP_006721579.2:p.Phe421Tyr
XM_011523829.2:c.1262T>A XP_011522131.1:p.Phe421Tyr
XM_011523830.2:c.1262T>A XP_011522132.1:p.Phe421Tyr
XM_024450741.1:c.1262T>A XP_024306509.1:p.Phe421Tyr
XR_934021.2:n.1321T>A
XR_934022.2:n.1321T>A
XR_934023.2:n.1321T>A
NM_000018.4:c.1262T>A MANE Select NP_000009.1:p.Phe421Tyr
NM_001033859.3:c.1196T>A NP_001029031.1:p.Phe399Tyr
NM_001270447.2:c.1331T>A NP_001257376.1:p.Phe444Tyr
NM_001270448.2:c.1034T>A NP_001257377.1:p.Phe345Tyr
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