Canonical Allele Identifier: CA2245710631

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7223206C= , CM000679.2:g.7223206C=	GRCh38
NC_000017.10:g.7126525C= , CM000679.1:g.7126525C=	GRCh37
NC_000017.9:g.7067249C=	NCBI36
NG_007975.1:g.8373C=
NG_008391.2:g.1845G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1151C= MANE Select	ENSP00000349297.5:p.Ala384=
ENST00000322910.9:c.*1106C=	ENSP00000325395.5:n.*1106C=
ENST00000350303.9:c.1085C=	ENSP00000344152.5:p.Ala362=
ENST00000356839.9:c.1151C=	ENSP00000349297.5:p.Ala384=
ENST00000542255.6:c.9C=
ENST00000543245.6:c.1220C=	ENSP00000438689.2:p.Ala407=
ENST00000578579.2:n.100C=
ENST00000578824.5:n.567C=
ENST00000579425.5:n.175C=
ENST00000582379.1:n.802C=
ENST00000583858.5:c.180C=
ENST00000585203.6:n.359C=
NM_000018.3:c.1151C=	NP_000009.1:p.Ala384=
NM_001033859.2:c.1085C=	NP_001029031.1:p.Ala362=
NM_001270447.1:c.1220C=	NP_001257376.1:p.Ala407=
NM_001270448.1:c.923C=	NP_001257377.1:p.Ala308=
XM_006721516.2:c.1151C=	XP_006721579.2:p.Ala384=
XM_011523829.1:c.1151C=	XP_011522131.1:p.Ala384=
XM_011523830.1:c.1151C=	XP_011522132.1:p.Ala384=
XR_934021.1:n.1258C=
XR_934022.1:n.1258C=
XR_934023.1:n.1258C=
XM_006721516.3:c.1151C=	XP_006721579.2:p.Ala384=
XM_011523829.2:c.1151C=	XP_011522131.1:p.Ala384=
XM_011523830.2:c.1151C=	XP_011522132.1:p.Ala384=
XM_024450741.1:c.1151C=	XP_024306509.1:p.Ala384=
XR_934021.2:n.1210C=
XR_934022.2:n.1210C=
XR_934023.2:n.1210C=
NM_000018.4:c.1151C= MANE Select	NP_000009.1:p.Ala384=
NM_001033859.3:c.1085C=	NP_001029031.1:p.Ala362=
NM_001270447.2:c.1220C=	NP_001257376.1:p.Ala407=
NM_001270448.2:c.923C=	NP_001257377.1:p.Ala308=