Canonical Allele Identifier: CA2245699037

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7220810C= , CM000679.2:g.7220810C=	GRCh38
NC_000017.10:g.7124129C= , CM000679.1:g.7124129C=	GRCh37
NC_000017.9:g.7064853C=	NCBI36
NG_007975.1:g.5977C=
NG_008391.2:g.4241G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.322C= MANE Select	ENSP00000349297.5:p.Pro108=
ENST00000322910.9:c.*277C=	ENSP00000325395.5:n.*277C=
ENST00000350303.9:c.256C=	ENSP00000344152.5:p.Pro86=
ENST00000356839.9:c.322C=	ENSP00000349297.5:p.Pro108=
ENST00000543245.6:c.391C=	ENSP00000438689.2:p.Pro131=
ENST00000577191.5:n.399C=
ENST00000577433.5:n.530C=
ENST00000577857.5:n.273C=
ENST00000579286.5:n.503C=
ENST00000579886.2:c.202-135C=	ENSP00000463246.1:n.202-135C=
ENST00000580365.1:n.53C=
ENST00000581378.5:c.21C=
ENST00000581562.5:n.369C=
ENST00000582056.5:n.412C=
ENST00000582166.1:n.210C=
ENST00000582356.5:n.521C=
ENST00000583312.5:c.322C=	ENSP00000467920.1:p.Pro108=
ENST00000584103.5:c.322C=	ENSP00000465353.1:p.Pro108=
NM_000018.3:c.322C=	NP_000009.1:p.Pro108=
NM_001033859.2:c.256C=	NP_001029031.1:p.Pro86=
NM_001270447.1:c.391C=	NP_001257376.1:p.Pro131=
NM_001270448.1:c.94C=	NP_001257377.1:p.Pro32=
XM_006721516.2:c.322C=	XP_006721579.2:p.Pro108=
XM_011523829.1:c.322C=	XP_011522131.1:p.Pro108=
XM_011523830.1:c.322C=	XP_011522132.1:p.Pro108=
XR_934021.1:n.429C=
XR_934022.1:n.429C=
XR_934023.1:n.429C=
XM_006721516.3:c.322C=	XP_006721579.2:p.Pro108=
XM_011523829.2:c.322C=	XP_011522131.1:p.Pro108=
XM_011523830.2:c.322C=	XP_011522132.1:p.Pro108=
XM_024450741.1:c.322C=	XP_024306509.1:p.Pro108=
XR_934021.2:n.381C=
XR_934022.2:n.381C=
XR_934023.2:n.381C=
NM_000018.4:c.322C= MANE Select	NP_000009.1:p.Pro108=
NM_001033859.3:c.256C=	NP_001029031.1:p.Pro86=
NM_001270447.2:c.391C=	NP_001257376.1:p.Pro131=
NM_001270448.2:c.94C=	NP_001257377.1:p.Pro32=