Canonical Allele Identifier: CA2245700616

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7221819_7221822delinsGGTT , CM000679.2:g.7221819_7221822delinsGGTT	GRCh38
NC_000017.10:g.7125138_7125141delinsGGTT , CM000679.1:g.7125138_7125141delinsGGTT	GRCh37
NC_000017.9:g.7065862_7065865delinsGGTT	NCBI36
NG_007975.1:g.6986_6989delinsGGTT
NG_008391.2:g.3229_3232delinsAACC

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.623-133_623-130delinsGGTT MANE Select	ENSP00000349297.5:n.623-133_623-130delinsGGTT
ENST00000322910.9:c.*578-133_*578-130delinsGGTT	ENSP00000325395.5:n.*578-133_*578-130delinsGGTT
ENST00000350303.9:c.557-133_557-130delinsGGTT	ENSP00000344152.5:n.557-133_557-130delinsGGTT
ENST00000356839.9:c.623-133_623-130delinsGGTT	ENSP00000349297.5:n.623-133_623-130delinsGGTT
ENST00000543245.6:c.692-133_692-130delinsGGTT	ENSP00000438689.2:n.692-133_692-130delinsGGTT
ENST00000577191.5:n.700-133_700-130delinsGGTT
ENST00000577857.5:n.439-133_439-130delinsGGTT
ENST00000579286.5:n.804-133_804-130delinsGGTT
ENST00000579886.2:c.461-133_461-130delinsGGTT	ENSP00000463246.1:n.461-133_461-130delinsGGTT
ENST00000580365.1:n.354-133_354-130delinsGGTT
ENST00000581378.5:c.341-133_341-130delinsGGTT
ENST00000581562.5:n.525-133_525-130delinsGGTT
ENST00000583312.5:c.623-118_623-115delinsGGTT	ENSP00000467920.1:n.623-118_623-115delinsGGTT
ENST00000583760.1:n.405-133_405-130delinsGGTT
NM_000018.3:c.623-133_623-130delinsGGTT	NP_000009.1:n.623-133_623-130delinsGGTT
NM_001033859.2:c.557-133_557-130delinsGGTT	NP_001029031.1:n.557-133_557-130delinsGGTT
NM_001270447.1:c.692-133_692-130delinsGGTT	NP_001257376.1:n.692-133_692-130delinsGGTT
NM_001270448.1:c.395-133_395-130delinsGGTT	NP_001257377.1:n.395-133_395-130delinsGGTT
XM_006721516.2:c.623-133_623-130delinsGGTT	XP_006721579.2:n.623-133_623-130delinsGGTT
XM_011523829.1:c.623-133_623-130delinsGGTT	XP_011522131.1:n.623-133_623-130delinsGGTT
XM_011523830.1:c.623-133_623-130delinsGGTT	XP_011522132.1:n.623-133_623-130delinsGGTT
XR_934021.1:n.730-133_730-130delinsGGTT
XR_934022.1:n.730-133_730-130delinsGGTT
XR_934023.1:n.730-133_730-130delinsGGTT
XM_006721516.3:c.623-133_623-130delinsGGTT	XP_006721579.2:n.623-133_623-130delinsGGTT
XM_011523829.2:c.623-133_623-130delinsGGTT	XP_011522131.1:n.623-133_623-130delinsGGTT
XM_011523830.2:c.623-133_623-130delinsGGTT	XP_011522132.1:n.623-133_623-130delinsGGTT
XM_024450741.1:c.623-133_623-130delinsGGTT	XP_024306509.1:n.623-133_623-130delinsGGTT
XR_934021.2:n.682-133_682-130delinsGGTT
XR_934022.2:n.682-133_682-130delinsGGTT
XR_934023.2:n.682-133_682-130delinsGGTT
NM_000018.4:c.623-133_623-130delinsGGTT MANE Select	NP_000009.1:n.623-133_623-130delinsGGTT
NM_001033859.3:c.557-133_557-130delinsGGTT	NP_001029031.1:n.557-133_557-130delinsGGTT
NM_001270447.2:c.692-133_692-130delinsGGTT	NP_001257376.1:n.692-133_692-130delinsGGTT
NM_001270448.2:c.395-133_395-130delinsGGTT	NP_001257377.1:n.395-133_395-130delinsGGTT