Canonical Allele Identifier: CA2245700219
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221602A= , CM000679.2:g.7221602A= GRCh38
NC_000017.10:g.7124921A= , CM000679.1:g.7124921A= GRCh37
NC_000017.9:g.7065645A= NCBI36
NG_007975.1:g.6769A=
NG_008391.2:g.3449T=

Transcript Alleles

HGVS Amino-acid change
ENST00000356839.10:c.542A= MANE Select ENSP00000349297.5:p.His181=
ENST00000322910.9:c.*497A= ENSP00000325395.5:n.*497A=
ENST00000350303.9:c.476A= ENSP00000344152.5:p.His159=
ENST00000356839.9:c.542A= ENSP00000349297.5:p.His181=
ENST00000543245.6:c.611A= ENSP00000438689.2:p.His204=
ENST00000577191.5:n.619A=
ENST00000577433.5:n.750A=
ENST00000577857.5:n.358A=
ENST00000579286.5:n.723A=
ENST00000579886.2:c.380A= ENSP00000463246.1:p.His127=
ENST00000580365.1:n.273A=
ENST00000581378.5:c.260A=
ENST00000581562.5:n.525-350A=
ENST00000582166.1:n.523A=
ENST00000583312.5:c.542A= ENSP00000467920.1:p.His181=
ENST00000583760.1:n.324A=
NM_000018.3:c.542A= NP_000009.1:p.His181=
NM_001033859.2:c.476A= NP_001029031.1:p.His159=
NM_001270447.1:c.611A= NP_001257376.1:p.His204=
NM_001270448.1:c.314A= NP_001257377.1:p.His105=
XM_006721516.2:c.542A= XP_006721579.2:p.His181=
XM_011523829.1:c.542A= XP_011522131.1:p.His181=
XM_011523830.1:c.542A= XP_011522132.1:p.His181=
XR_934021.1:n.649A=
XR_934022.1:n.649A=
XR_934023.1:n.649A=
XM_006721516.3:c.542A= XP_006721579.2:p.His181=
XM_011523829.2:c.542A= XP_011522131.1:p.His181=
XM_011523830.2:c.542A= XP_011522132.1:p.His181=
XM_024450741.1:c.542A= XP_024306509.1:p.His181=
XR_934021.2:n.601A=
XR_934022.2:n.601A=
XR_934023.2:n.601A=
NM_000018.4:c.542A= MANE Select NP_000009.1:p.His181=
NM_001033859.3:c.476A= NP_001029031.1:p.His159=
NM_001270447.2:c.611A= NP_001257376.1:p.His204=
NM_001270448.2:c.314A= NP_001257377.1:p.His105=