Canonical Allele Identifier: CA2245700605

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7221808C= , CM000679.2:g.7221808C=	GRCh38
NC_000017.10:g.7125127C= , CM000679.1:g.7125127C=	GRCh37
NC_000017.9:g.7065851C=	NCBI36
NG_007975.1:g.6975C=
NG_008391.2:g.3243G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.622+126C= MANE Select	ENSP00000349297.5:n.622+126C=
ENST00000322910.9:c.*577+126C=	ENSP00000325395.5:n.*577+126C=
ENST00000350303.9:c.556+126C=	ENSP00000344152.5:n.556+126C=
ENST00000356839.9:c.622+126C=	ENSP00000349297.5:n.622+126C=
ENST00000543245.6:c.691+126C=	ENSP00000438689.2:n.691+126C=
ENST00000577191.5:n.699+126C=
ENST00000577857.5:n.438+126C=
ENST00000579286.5:n.803+126C=
ENST00000579886.2:c.460+126C=	ENSP00000463246.1:n.460+126C=
ENST00000580365.1:n.353+126C=
ENST00000581378.5:c.340+126C=
ENST00000581562.5:n.525-144C=
ENST00000583312.5:c.622+126C=	ENSP00000467920.1:n.622+126C=
ENST00000583760.1:n.404+126C=
NM_000018.3:c.622+126C=	NP_000009.1:n.622+126C=
NM_001033859.2:c.556+126C=	NP_001029031.1:n.556+126C=
NM_001270447.1:c.691+126C=	NP_001257376.1:n.691+126C=
NM_001270448.1:c.394+126C=	NP_001257377.1:n.394+126C=
XM_006721516.2:c.622+126C=	XP_006721579.2:n.622+126C=
XM_011523829.1:c.622+126C=	XP_011522131.1:n.622+126C=
XM_011523830.1:c.622+126C=	XP_011522132.1:n.622+126C=
XR_934021.1:n.729+126C=
XR_934022.1:n.729+126C=
XR_934023.1:n.729+126C=
XM_006721516.3:c.622+126C=	XP_006721579.2:n.622+126C=
XM_011523829.2:c.622+126C=	XP_011522131.1:n.622+126C=
XM_011523830.2:c.622+126C=	XP_011522132.1:n.622+126C=
XM_024450741.1:c.622+126C=	XP_024306509.1:n.622+126C=
XR_934021.2:n.681+126C=
XR_934022.2:n.681+126C=
XR_934023.2:n.681+126C=
NM_000018.4:c.622+126C= MANE Select	NP_000009.1:n.622+126C=
NM_001033859.3:c.556+126C=	NP_001029031.1:n.556+126C=
NM_001270447.2:c.691+126C=	NP_001257376.1:n.691+126C=
NM_001270448.2:c.394+126C=	NP_001257377.1:n.394+126C=