Canonical Allele Identifier: CA2245711849

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7223772C= , CM000679.2:g.7223772C=	GRCh38
NC_000017.10:g.7127091C= , CM000679.1:g.7127091C=	GRCh37
NC_000017.9:g.7067815C=	NCBI36
NG_007975.1:g.8939C=
NG_008391.2:g.1279G=
NG_033038.1:g.15773G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1270-41C= MANE Select	ENSP00000349297.5:n.1270-41C=
ENST00000322910.9:c.*1225-41C=	ENSP00000325395.5:n.*1225-41C=
ENST00000350303.9:c.1204-41C=	ENSP00000344152.5:n.1204-41C=
ENST00000356839.9:c.1270-41C=	ENSP00000349297.5:n.1270-41C=
ENST00000542255.6:c.128-41C=
ENST00000543245.6:c.1339-41C=	ENSP00000438689.2:n.1339-41C=
ENST00000578579.2:n.441-41C=
ENST00000578711.1:n.268C=
ENST00000578824.5:n.686-41C=
ENST00000579425.5:n.294-41C=
ENST00000579546.1:c.107-41C=
ENST00000583850.5:n.45-41C=
ENST00000583858.5:c.299-41C=
ENST00000585203.6:n.478-41C=
NM_000018.3:c.1270-41C=	NP_000009.1:n.1270-41C=
NM_001033859.2:c.1204-41C=	NP_001029031.1:n.1204-41C=
NM_001270447.1:c.1339-41C=	NP_001257376.1:n.1339-41C=
NM_001270448.1:c.1042-41C=	NP_001257377.1:n.1042-41C=
XM_006721516.2:c.1270-41C=	XP_006721579.2:n.1270-41C=
XM_011523829.1:c.1270-41C=	XP_011522131.1:n.1270-41C=
XM_011523830.1:c.1270-41C=	XP_011522132.1:n.1270-41C=
XR_934021.1:n.1377-41C=
XR_934022.1:n.1377-41C=
XR_934023.1:n.1377-41C=
XM_006721516.3:c.1270-41C=	XP_006721579.2:n.1270-41C=
XM_011523829.2:c.1270-41C=	XP_011522131.1:n.1270-41C=
XM_011523830.2:c.1270-41C=	XP_011522132.1:n.1270-41C=
XM_024450741.1:c.1270-41C=	XP_024306509.1:n.1270-41C=
XR_934021.2:n.1329-41C=
XR_934022.2:n.1329-41C=
XR_934023.2:n.1329-41C=
NM_000018.4:c.1270-41C= MANE Select	NP_000009.1:n.1270-41C=
NM_001033859.3:c.1204-41C=	NP_001029031.1:n.1204-41C=
NM_001270447.2:c.1339-41C=	NP_001257376.1:n.1339-41C=
NM_001270448.2:c.1042-41C=	NP_001257377.1:n.1042-41C=