Canonical Allele Identifier: CA2245700628

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7221835_7221836delinsAG , CM000679.2:g.7221835_7221836delinsAG	GRCh38
NC_000017.10:g.7125154_7125155delinsAG , CM000679.1:g.7125154_7125155delinsAG	GRCh37
NC_000017.9:g.7065878_7065879delinsAG	NCBI36
NG_007975.1:g.7002_7003delinsAG
NG_008391.2:g.3215_3216delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.623-117_623-116delinsAG MANE Select	ENSP00000349297.5:n.623-117_623-116delinsAG
ENST00000322910.9:c.*578-117_*578-116delinsAG	ENSP00000325395.5:n.*578-117_*578-116delinsAG
ENST00000350303.9:c.557-117_557-116delinsAG	ENSP00000344152.5:n.557-117_557-116delinsAG
ENST00000356839.9:c.623-117_623-116delinsAG	ENSP00000349297.5:n.623-117_623-116delinsAG
ENST00000543245.6:c.692-117_692-116delinsAG	ENSP00000438689.2:n.692-117_692-116delinsAG
ENST00000577191.5:n.700-117_700-116delinsAG
ENST00000577857.5:n.439-117_439-116delinsAG
ENST00000579286.5:n.804-117_804-116delinsAG
ENST00000579886.2:c.461-117_461-116delinsAG	ENSP00000463246.1:n.461-117_461-116delinsAG
ENST00000580365.1:n.354-117_354-116delinsAG
ENST00000581378.5:c.341-117_341-116delinsAG
ENST00000581562.5:n.525-117_525-116delinsAG
ENST00000583312.5:c.623-102_623-101delinsAG	ENSP00000467920.1:n.623-102_623-101delinsAG
ENST00000583760.1:n.405-117_405-116delinsAG
NM_000018.3:c.623-117_623-116delinsAG	NP_000009.1:n.623-117_623-116delinsAG
NM_001033859.2:c.557-117_557-116delinsAG	NP_001029031.1:n.557-117_557-116delinsAG
NM_001270447.1:c.692-117_692-116delinsAG	NP_001257376.1:n.692-117_692-116delinsAG
NM_001270448.1:c.395-117_395-116delinsAG	NP_001257377.1:n.395-117_395-116delinsAG
XM_006721516.2:c.623-117_623-116delinsAG	XP_006721579.2:n.623-117_623-116delinsAG
XM_011523829.1:c.623-117_623-116delinsAG	XP_011522131.1:n.623-117_623-116delinsAG
XM_011523830.1:c.623-117_623-116delinsAG	XP_011522132.1:n.623-117_623-116delinsAG
XR_934021.1:n.730-117_730-116delinsAG
XR_934022.1:n.730-117_730-116delinsAG
XR_934023.1:n.730-117_730-116delinsAG
XM_006721516.3:c.623-117_623-116delinsAG	XP_006721579.2:n.623-117_623-116delinsAG
XM_011523829.2:c.623-117_623-116delinsAG	XP_011522131.1:n.623-117_623-116delinsAG
XM_011523830.2:c.623-117_623-116delinsAG	XP_011522132.1:n.623-117_623-116delinsAG
XM_024450741.1:c.623-117_623-116delinsAG	XP_024306509.1:n.623-117_623-116delinsAG
XR_934021.2:n.682-117_682-116delinsAG
XR_934022.2:n.682-117_682-116delinsAG
XR_934023.2:n.682-117_682-116delinsAG
NM_000018.4:c.623-117_623-116delinsAG MANE Select	NP_000009.1:n.623-117_623-116delinsAG
NM_001033859.3:c.557-117_557-116delinsAG	NP_001029031.1:n.557-117_557-116delinsAG
NM_001270447.2:c.692-117_692-116delinsAG	NP_001257376.1:n.692-117_692-116delinsAG
NM_001270448.2:c.395-117_395-116delinsAG	NP_001257377.1:n.395-117_395-116delinsAG