Canonical Allele Identifier: CA2245700847

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7221984C= , CM000679.2:g.7221984C=	GRCh38
NC_000017.10:g.7125303C= , CM000679.1:g.7125303C=	GRCh37
NC_000017.9:g.7066027C=	NCBI36
NG_007975.1:g.7151C=
NG_008391.2:g.3067G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.655C= MANE Select	ENSP00000349297.5:p.Pro219=
ENST00000322910.9:c.*610C=	ENSP00000325395.5:n.*610C=
ENST00000350303.9:c.589C=	ENSP00000344152.5:p.Pro197=
ENST00000356839.9:c.655C=	ENSP00000349297.5:p.Pro219=
ENST00000543245.6:c.724C=	ENSP00000438689.2:p.Pro242=
ENST00000577191.5:n.732C=
ENST00000577857.5:n.471C=
ENST00000579286.5:n.836C=
ENST00000580365.1:n.386C=
ENST00000581378.5:c.373C=
ENST00000581562.5:n.557C=
ENST00000582379.1:n.39C=
ENST00000583312.5:c.670C=	ENSP00000467920.1:p.Pro224=
ENST00000583760.1:n.437C=
NM_000018.3:c.655C=	NP_000009.1:p.Pro219=
NM_001033859.2:c.589C=	NP_001029031.1:p.Pro197=
NM_001270447.1:c.724C=	NP_001257376.1:p.Pro242=
NM_001270448.1:c.427C=	NP_001257377.1:p.Pro143=
XM_006721516.2:c.655C=	XP_006721579.2:p.Pro219=
XM_011523829.1:c.655C=	XP_011522131.1:p.Pro219=
XM_011523830.1:c.655C=	XP_011522132.1:p.Pro219=
XR_934021.1:n.762C=
XR_934022.1:n.762C=
XR_934023.1:n.762C=
XM_006721516.3:c.655C=	XP_006721579.2:p.Pro219=
XM_011523829.2:c.655C=	XP_011522131.1:p.Pro219=
XM_011523830.2:c.655C=	XP_011522132.1:p.Pro219=
XM_024450741.1:c.655C=	XP_024306509.1:p.Pro219=
XR_934021.2:n.714C=
XR_934022.2:n.714C=
XR_934023.2:n.714C=
NM_000018.4:c.655C= MANE Select	NP_000009.1:p.Pro219=
NM_001033859.3:c.589C=	NP_001029031.1:p.Pro197=
NM_001270447.2:c.724C=	NP_001257376.1:p.Pro242=
NM_001270448.2:c.427C=	NP_001257377.1:p.Pro143=