Canonical Allele Identifier: CA2245700960

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7222035C= , CM000679.2:g.7222035C=	GRCh38
NC_000017.10:g.7125354C= , CM000679.1:g.7125354C=	GRCh37
NC_000017.9:g.7066078C=	NCBI36
NG_007975.1:g.7202C=
NG_008391.2:g.3016G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.706C= MANE Select	ENSP00000349297.5:p.Pro236=
ENST00000322910.9:c.*661C=	ENSP00000325395.5:n.*661C=
ENST00000350303.9:c.640C=	ENSP00000344152.5:p.Pro214=
ENST00000356839.9:c.706C=	ENSP00000349297.5:p.Pro236=
ENST00000543245.6:c.775C=	ENSP00000438689.2:p.Pro259=
ENST00000577191.5:n.783C=
ENST00000577857.5:n.522C=
ENST00000579286.5:n.887C=
ENST00000580365.1:n.437C=
ENST00000581378.5:c.424C=
ENST00000582379.1:n.90C=
ENST00000583760.1:n.488C=
NM_000018.3:c.706C=	NP_000009.1:p.Pro236=
NM_001033859.2:c.640C=	NP_001029031.1:p.Pro214=
NM_001270447.1:c.775C=	NP_001257376.1:p.Pro259=
NM_001270448.1:c.478C=	NP_001257377.1:p.Pro160=
XM_006721516.2:c.706C=	XP_006721579.2:p.Pro236=
XM_011523829.1:c.706C=	XP_011522131.1:p.Pro236=
XM_011523830.1:c.706C=	XP_011522132.1:p.Pro236=
XR_934021.1:n.813C=
XR_934022.1:n.813C=
XR_934023.1:n.813C=
XM_006721516.3:c.706C=	XP_006721579.2:p.Pro236=
XM_011523829.2:c.706C=	XP_011522131.1:p.Pro236=
XM_011523830.2:c.706C=	XP_011522132.1:p.Pro236=
XM_024450741.1:c.706C=	XP_024306509.1:p.Pro236=
XR_934021.2:n.765C=
XR_934022.2:n.765C=
XR_934023.2:n.765C=
NM_000018.4:c.706C= MANE Select	NP_000009.1:p.Pro236=
NM_001033859.3:c.640C=	NP_001029031.1:p.Pro214=
NM_001270447.2:c.775C=	NP_001257376.1:p.Pro259=
NM_001270448.2:c.478C=	NP_001257377.1:p.Pro160=