Canonical Allele Identifier: CA2245701136

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7222119A= , CM000679.2:g.7222119A=	GRCh38
NC_000017.10:g.7125438A= , CM000679.1:g.7125438A=	GRCh37
NC_000017.9:g.7066162A=	NCBI36
NG_007975.1:g.7286A=
NG_008391.2:g.2932T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.752+38A= MANE Select	ENSP00000349297.5:n.752+38A=
ENST00000322910.9:c.*707+38A=	ENSP00000325395.5:n.*707+38A=
ENST00000350303.9:c.686+38A=	ENSP00000344152.5:n.686+38A=
ENST00000356839.9:c.752+38A=	ENSP00000349297.5:n.752+38A=
ENST00000543245.6:c.821+38A=	ENSP00000438689.2:n.821+38A=
ENST00000577191.5:n.867A=
ENST00000581378.5:c.470+38A=
ENST00000582379.1:n.136+38A=
ENST00000583760.1:n.572A=
NM_000018.3:c.752+38A=	NP_000009.1:n.752+38A=
NM_001033859.2:c.686+38A=	NP_001029031.1:n.686+38A=
NM_001270447.1:c.821+38A=	NP_001257376.1:n.821+38A=
NM_001270448.1:c.524+38A=	NP_001257377.1:n.524+38A=
XM_006721516.2:c.752+38A=	XP_006721579.2:n.752+38A=
XM_011523829.1:c.752+38A=	XP_011522131.1:n.752+38A=
XM_011523830.1:c.752+38A=	XP_011522132.1:n.752+38A=
XR_934021.1:n.859+38A=
XR_934022.1:n.859+38A=
XR_934023.1:n.859+38A=
XM_006721516.3:c.752+38A=	XP_006721579.2:n.752+38A=
XM_011523829.2:c.752+38A=	XP_011522131.1:n.752+38A=
XM_011523830.2:c.752+38A=	XP_011522132.1:n.752+38A=
XM_024450741.1:c.752+38A=	XP_024306509.1:n.752+38A=
XR_934021.2:n.811+38A=
XR_934022.2:n.811+38A=
XR_934023.2:n.811+38A=
NM_000018.4:c.752+38A= MANE Select	NP_000009.1:n.752+38A=
NM_001033859.3:c.686+38A=	NP_001029031.1:n.686+38A=
NM_001270447.2:c.821+38A=	NP_001257376.1:n.821+38A=
NM_001270448.2:c.524+38A=	NP_001257377.1:n.524+38A=