Canonical Allele Identifier: CA2245701151

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7222140C= , CM000679.2:g.7222140C=	GRCh38
NC_000017.10:g.7125459C= , CM000679.1:g.7125459C=	GRCh37
NC_000017.9:g.7066183C=	NCBI36
NG_007975.1:g.7307C=
NG_008391.2:g.2911G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.753-37C= MANE Select	ENSP00000349297.5:n.753-37C=
ENST00000322910.9:c.*708-37C=	ENSP00000325395.5:n.*708-37C=
ENST00000350303.9:c.687-37C=	ENSP00000344152.5:n.687-37C=
ENST00000356839.9:c.753-37C=	ENSP00000349297.5:n.753-37C=
ENST00000543245.6:c.822-37C=	ENSP00000438689.2:n.822-37C=
ENST00000577191.5:n.888C=
ENST00000581378.5:c.471-37C=
ENST00000582379.1:n.137-37C=
ENST00000583760.1:n.593C=
NM_000018.3:c.753-37C=	NP_000009.1:n.753-37C=
NM_001033859.2:c.687-37C=	NP_001029031.1:n.687-37C=
NM_001270447.1:c.822-37C=	NP_001257376.1:n.822-37C=
NM_001270448.1:c.525-37C=	NP_001257377.1:n.525-37C=
XM_006721516.2:c.753-37C=	XP_006721579.2:n.753-37C=
XM_011523829.1:c.753-37C=	XP_011522131.1:n.753-37C=
XM_011523830.1:c.753-37C=	XP_011522132.1:n.753-37C=
XR_934021.1:n.860-37C=
XR_934022.1:n.860-37C=
XR_934023.1:n.860-37C=
XM_006721516.3:c.753-37C=	XP_006721579.2:n.753-37C=
XM_011523829.2:c.753-37C=	XP_011522131.1:n.753-37C=
XM_011523830.2:c.753-37C=	XP_011522132.1:n.753-37C=
XM_024450741.1:c.753-37C=	XP_024306509.1:n.753-37C=
XR_934021.2:n.812-37C=
XR_934022.2:n.812-37C=
XR_934023.2:n.812-37C=
NM_000018.4:c.753-37C= MANE Select	NP_000009.1:n.753-37C=
NM_001033859.3:c.687-37C=	NP_001029031.1:n.687-37C=
NM_001270447.2:c.822-37C=	NP_001257376.1:n.822-37C=
NM_001270448.2:c.525-37C=	NP_001257377.1:n.525-37C=