Canonical Allele Identifier: CA2245698679
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7220663C= , CM000679.2:g.7220663C= GRCh38
NC_000017.10:g.7123982C= , CM000679.1:g.7123982C= GRCh37
NC_000017.9:g.7064706C= NCBI36
NG_007975.1:g.5830C=
NG_008391.2:g.4388G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.264C= MANE Select ENSP00000349297.5:p.Phe88=
ENST00000322910.9:c.*219C= ENSP00000325395.5:n.*219C=
ENST00000350303.9:c.198C= ENSP00000344152.5:p.Phe66=
ENST00000356839.9:c.264C= ENSP00000349297.5:p.Phe88=
ENST00000543245.6:c.333C= ENSP00000438689.2:p.Phe111=
ENST00000577191.5:n.341C=
ENST00000577433.5:n.472C=
ENST00000577857.5:n.229-103C=
ENST00000578269.5:n.711C=
ENST00000578421.1:n.472C=
ENST00000579286.5:n.445C=
ENST00000579886.2:c.201+137C= ENSP00000463246.1:n.201+137C=
ENST00000580263.5:n.428C=
ENST00000581562.5:n.311C=
ENST00000582056.5:n.354C=
ENST00000582166.1:n.152C=
ENST00000582356.5:n.463C=
ENST00000583312.5:c.264C= ENSP00000467920.1:p.Phe88=
ENST00000584103.5:c.264C= ENSP00000465353.1:p.Phe88=
NM_000018.3:c.264C= NP_000009.1:p.Phe88=
NM_001033859.2:c.198C= NP_001029031.1:p.Phe66=
NM_001270447.1:c.333C= NP_001257376.1:p.Phe111=
NM_001270448.1:c.36C= NP_001257377.1:p.Phe12=
XM_006721516.2:c.264C= XP_006721579.2:p.Phe88=
XM_011523829.1:c.264C= XP_011522131.1:p.Phe88=
XM_011523830.1:c.264C= XP_011522132.1:p.Phe88=
XR_934021.1:n.371C=
XR_934022.1:n.371C=
XR_934023.1:n.371C=
XM_006721516.3:c.264C= XP_006721579.2:p.Phe88=
XM_011523829.2:c.264C= XP_011522131.1:p.Phe88=
XM_011523830.2:c.264C= XP_011522132.1:p.Phe88=
XM_024450741.1:c.264C= XP_024306509.1:p.Phe88=
XR_934021.2:n.323C=
XR_934022.2:n.323C=
XR_934023.2:n.323C=
NM_000018.4:c.264C= MANE Select NP_000009.1:p.Phe88=
NM_001033859.3:c.198C= NP_001029031.1:p.Phe66=
NM_001270447.2:c.333C= NP_001257376.1:p.Phe111=
NM_001270448.2:c.36C= NP_001257377.1:p.Phe12=