Canonical Allele Identifier: CA397722614
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7220826T>A , CM000679.2:g.7220826T>A GRCh38
NC_000017.10:g.7124145T>A , CM000679.1:g.7124145T>A GRCh37
NC_000017.9:g.7064869T>A NCBI36
NG_007975.1:g.5993T>A
NG_008391.2:g.4225A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.338T>A MANE Select ENSP00000349297.5:p.Phe113Tyr
ENST00000322910.9:c.*293T>A ENSP00000325395.5:n.*293T>A
ENST00000350303.9:c.272T>A ENSP00000344152.5:p.Phe91Tyr
ENST00000356839.9:c.338T>A ENSP00000349297.5:p.Phe113Tyr
ENST00000543245.6:c.407T>A ENSP00000438689.2:p.Phe136Tyr
ENST00000577191.5:n.415T>A
ENST00000577433.5:n.546T>A
ENST00000577857.5:n.289T>A
ENST00000579286.5:n.519T>A
ENST00000579886.2:c.202-119T>A ENSP00000463246.1:n.202-119T>A
ENST00000580365.1:n.69T>A
ENST00000581378.5:c.37T>A
ENST00000581562.5:n.385T>A
ENST00000582056.5:n.428T>A
ENST00000582166.1:n.226T>A
ENST00000582356.5:n.537T>A
ENST00000583312.5:c.338T>A ENSP00000467920.1:p.Phe113Tyr
ENST00000584103.5:c.338T>A ENSP00000465353.1:p.Phe113Tyr
NM_000018.3:c.338T>A NP_000009.1:p.Phe113Tyr
NM_001033859.2:c.272T>A NP_001029031.1:p.Phe91Tyr
NM_001270447.1:c.407T>A NP_001257376.1:p.Phe136Tyr
NM_001270448.1:c.110T>A NP_001257377.1:p.Phe37Tyr
XM_006721516.2:c.338T>A XP_006721579.2:p.Phe113Tyr
XM_011523829.1:c.338T>A XP_011522131.1:p.Phe113Tyr
XM_011523830.1:c.338T>A XP_011522132.1:p.Phe113Tyr
XR_934021.1:n.445T>A
XR_934022.1:n.445T>A
XR_934023.1:n.445T>A
XM_006721516.3:c.338T>A XP_006721579.2:p.Phe113Tyr
XM_011523829.2:c.338T>A XP_011522131.1:p.Phe113Tyr
XM_011523830.2:c.338T>A XP_011522132.1:p.Phe113Tyr
XM_024450741.1:c.338T>A XP_024306509.1:p.Phe113Tyr
XR_934021.2:n.397T>A
XR_934022.2:n.397T>A
XR_934023.2:n.397T>A
NM_000018.4:c.338T>A MANE Select NP_000009.1:p.Phe113Tyr
NM_001033859.3:c.272T>A NP_001029031.1:p.Phe91Tyr
NM_001270447.2:c.407T>A NP_001257376.1:p.Phe136Tyr
NM_001270448.2:c.110T>A NP_001257377.1:p.Phe37Tyr