Canonical Allele Identifier: CA2245699061

Gene: ACADVL

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.338T= MANE Select	ENSP00000349297.5:p.Phe113=
ENST00000322910.9:c.*293T=	ENSP00000325395.5:n.*293T=
ENST00000350303.9:c.272T=	ENSP00000344152.5:p.Phe91=
ENST00000356839.9:c.338T=	ENSP00000349297.5:p.Phe113=
ENST00000543245.6:c.407T=	ENSP00000438689.2:p.Phe136=
ENST00000577191.5:n.415T=
ENST00000577433.5:n.546T=
ENST00000577857.5:n.289T=
ENST00000579286.5:n.519T=
ENST00000579886.2:c.202-119T=	ENSP00000463246.1:n.202-119T=
ENST00000580365.1:n.69T=
ENST00000581378.5:c.37T=
ENST00000581562.5:n.385T=
ENST00000582056.5:n.428T=
ENST00000582166.1:n.226T=
ENST00000582356.5:n.537T=
ENST00000583312.5:c.338T=	ENSP00000467920.1:p.Phe113=
ENST00000584103.5:c.338T=	ENSP00000465353.1:p.Phe113=
NM_000018.3:c.338T=	NP_000009.1:p.Phe113=
NM_001033859.2:c.272T=	NP_001029031.1:p.Phe91=
NM_001270447.1:c.407T=	NP_001257376.1:p.Phe136=
NM_001270448.1:c.110T=	NP_001257377.1:p.Phe37=
XM_006721516.2:c.338T=	XP_006721579.2:p.Phe113=
XM_011523829.1:c.338T=	XP_011522131.1:p.Phe113=
XM_011523830.1:c.338T=	XP_011522132.1:p.Phe113=
XR_934021.1:n.445T=
XR_934022.1:n.445T=
XR_934023.1:n.445T=
XM_006721516.3:c.338T=	XP_006721579.2:p.Phe113=
XM_011523829.2:c.338T=	XP_011522131.1:p.Phe113=
XM_011523830.2:c.338T=	XP_011522132.1:p.Phe113=
XM_024450741.1:c.338T=	XP_024306509.1:p.Phe113=
XR_934021.2:n.397T=
XR_934022.2:n.397T=
XR_934023.2:n.397T=
NM_000018.4:c.338T= MANE Select	NP_000009.1:p.Phe113=
NM_001033859.3:c.272T=	NP_001029031.1:p.Phe91=
NM_001270447.2:c.407T=	NP_001257376.1:p.Phe136=
NM_001270448.2:c.110T=	NP_001257377.1:p.Phe37=