Canonical Allele Identifier: CA2245709747

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7222811G= , CM000679.2:g.7222811G=	GRCh38
NC_000017.10:g.7126130G= , CM000679.1:g.7126130G=	GRCh37
NC_000017.9:g.7066854G=	NCBI36
NG_007975.1:g.7978G=
NG_008391.2:g.2240C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1023G= MANE Select	ENSP00000349297.5:p.Arg341=
ENST00000322910.9:c.*978G=	ENSP00000325395.5:n.*978G=
ENST00000350303.9:c.957G=	ENSP00000344152.5:p.Arg319=
ENST00000356839.9:c.1023G=	ENSP00000349297.5:p.Arg341=
ENST00000543245.6:c.1092G=	ENSP00000438689.2:p.Arg364=
ENST00000578824.5:n.172G=
ENST00000581378.5:c.741G=
ENST00000582379.1:n.407G=
ENST00000583858.5:c.52G=
NM_000018.3:c.1023G=	NP_000009.1:p.Arg341=
NM_001033859.2:c.957G=	NP_001029031.1:p.Arg319=
NM_001270447.1:c.1092G=	NP_001257376.1:p.Arg364=
NM_001270448.1:c.795G=	NP_001257377.1:p.Arg265=
XM_006721516.2:c.1023G=	XP_006721579.2:p.Arg341=
XM_011523829.1:c.1023G=	XP_011522131.1:p.Arg341=
XM_011523830.1:c.1023G=	XP_011522132.1:p.Arg341=
XR_934021.1:n.1130G=
XR_934022.1:n.1130G=
XR_934023.1:n.1130G=
XM_006721516.3:c.1023G=	XP_006721579.2:p.Arg341=
XM_011523829.2:c.1023G=	XP_011522131.1:p.Arg341=
XM_011523830.2:c.1023G=	XP_011522132.1:p.Arg341=
XM_024450741.1:c.1023G=	XP_024306509.1:p.Arg341=
XR_934021.2:n.1082G=
XR_934022.2:n.1082G=
XR_934023.2:n.1082G=
NM_000018.4:c.1023G= MANE Select	NP_000009.1:p.Arg341=
NM_001033859.3:c.957G=	NP_001029031.1:p.Arg319=
NM_001270447.2:c.1092G=	NP_001257376.1:p.Arg364=
NM_001270448.2:c.795G=	NP_001257377.1:p.Arg265=