Canonical Allele Identifier: CA2245712225

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7223903G= , CM000679.2:g.7223903G=	GRCh38
NC_000017.10:g.7127222G= , CM000679.1:g.7127222G=	GRCh37
NC_000017.9:g.7067946G=	NCBI36
NG_007975.1:g.9070G=
NG_008391.2:g.1148C=
NG_033038.1:g.15642C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.1332+28G= MANE Select	ENSP00000349297.5:n.1332+28G=
ENST00000322910.9:c.*1287+28G=	ENSP00000325395.5:n.*1287+28G=
ENST00000350303.9:c.1266+28G=	ENSP00000344152.5:n.1266+28G=
ENST00000356839.9:c.1332+28G=	ENSP00000349297.5:n.1332+28G=
ENST00000542255.6:c.190+28G=
ENST00000543245.6:c.1401+28G=	ENSP00000438689.2:n.1401+28G=
ENST00000578711.1:n.399G=
ENST00000579425.5:n.384G=
ENST00000579546.1:c.169+28G=
ENST00000583074.5:n.51+28G=
ENST00000583850.5:n.107+28G=
ENST00000583858.5:c.361+28G=
ENST00000585203.6:n.523+45G=
NM_000018.3:c.1332+28G=	NP_000009.1:n.1332+28G=
NM_001033859.2:c.1266+28G=	NP_001029031.1:n.1266+28G=
NM_001270447.1:c.1401+28G=	NP_001257376.1:n.1401+28G=
NM_001270448.1:c.1104+28G=	NP_001257377.1:n.1104+28G=
XM_006721516.2:c.1332+28G=	XP_006721579.2:n.1332+28G=
XM_011523829.1:c.1332+28G=	XP_011522131.1:n.1332+28G=
XM_011523830.1:c.1332+28G=	XP_011522132.1:n.1332+28G=
XR_934021.1:n.1439+28G=
XR_934022.1:n.1439+28G=
XR_934023.1:n.1439+28G=
XM_006721516.3:c.1332+28G=	XP_006721579.2:n.1332+28G=
XM_011523829.2:c.1332+28G=	XP_011522131.1:n.1332+28G=
XM_011523830.2:c.1332+28G=	XP_011522132.1:n.1332+28G=
XM_024450741.1:c.1332+28G=	XP_024306509.1:n.1332+28G=
XR_934021.2:n.1391+28G=
XR_934022.2:n.1391+28G=
XR_934023.2:n.1391+28G=
NM_000018.4:c.1332+28G= MANE Select	NP_000009.1:n.1332+28G=
NM_001033859.3:c.1266+28G=	NP_001029031.1:n.1266+28G=
NM_001270447.2:c.1401+28G=	NP_001257376.1:n.1401+28G=
NM_001270448.2:c.1104+28G=	NP_001257377.1:n.1104+28G=