Canonical Allele Identifier: CA2245711120

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7223487_7223489delinsCAA , CM000679.2:g.7223487_7223489delinsCAA	GRCh38
NC_000017.10:g.7126806_7126808delinsCAA , CM000679.1:g.7126806_7126808delinsCAA	GRCh37
NC_000017.9:g.7067530_7067532delinsCAA	NCBI36
NG_007975.1:g.8654_8656delinsCAA
NG_008391.2:g.1562_1564delinsTTG
NG_033038.1:g.16056_16058delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1183-157_1183-155delinsCAA MANE Select	ENSP00000349297.5:n.1183-157_1183-155delinsCAA
ENST00000322910.9:c.*1138-157_*1138-155delinsCAA	ENSP00000325395.5:n.*1138-157_*1138-155delinsCAA
ENST00000350303.9:c.1117-157_1117-155delinsCAA	ENSP00000344152.5:n.1117-157_1117-155delinsCAA
ENST00000356839.9:c.1183-157_1183-155delinsCAA	ENSP00000349297.5:n.1183-157_1183-155delinsCAA
ENST00000542255.6:c.41-157_41-155delinsCAA
ENST00000543245.6:c.1252-157_1252-155delinsCAA	ENSP00000438689.2:n.1252-157_1252-155delinsCAA
ENST00000578579.2:n.197_199delinsCAA
ENST00000578824.5:n.599-157_599-155delinsCAA
ENST00000579425.5:n.207-157_207-155delinsCAA
ENST00000579546.1:c.20-157_20-155delinsCAA
ENST00000583858.5:c.212-157_212-155delinsCAA
ENST00000585203.6:n.391-157_391-155delinsCAA
NM_000018.3:c.1183-157_1183-155delinsCAA	NP_000009.1:n.1183-157_1183-155delinsCAA
NM_001033859.2:c.1117-157_1117-155delinsCAA	NP_001029031.1:n.1117-157_1117-155delinsCAA
NM_001270447.1:c.1252-157_1252-155delinsCAA	NP_001257376.1:n.1252-157_1252-155delinsCAA
NM_001270448.1:c.955-157_955-155delinsCAA	NP_001257377.1:n.955-157_955-155delinsCAA
XM_006721516.2:c.1183-157_1183-155delinsCAA	XP_006721579.2:n.1183-157_1183-155delinsCAA
XM_011523829.1:c.1183-157_1183-155delinsCAA	XP_011522131.1:n.1183-157_1183-155delinsCAA
XM_011523830.1:c.1183-157_1183-155delinsCAA	XP_011522132.1:n.1183-157_1183-155delinsCAA
XR_934021.1:n.1290-157_1290-155delinsCAA
XR_934022.1:n.1290-157_1290-155delinsCAA
XR_934023.1:n.1290-157_1290-155delinsCAA
XM_006721516.3:c.1183-157_1183-155delinsCAA	XP_006721579.2:n.1183-157_1183-155delinsCAA
XM_011523829.2:c.1183-157_1183-155delinsCAA	XP_011522131.1:n.1183-157_1183-155delinsCAA
XM_011523830.2:c.1183-157_1183-155delinsCAA	XP_011522132.1:n.1183-157_1183-155delinsCAA
XM_024450741.1:c.1183-157_1183-155delinsCAA	XP_024306509.1:n.1183-157_1183-155delinsCAA
XR_934021.2:n.1242-157_1242-155delinsCAA
XR_934022.2:n.1242-157_1242-155delinsCAA
XR_934023.2:n.1242-157_1242-155delinsCAA
NM_000018.4:c.1183-157_1183-155delinsCAA MANE Select	NP_000009.1:n.1183-157_1183-155delinsCAA
NM_001033859.3:c.1117-157_1117-155delinsCAA	NP_001029031.1:n.1117-157_1117-155delinsCAA
NM_001270447.2:c.1252-157_1252-155delinsCAA	NP_001257376.1:n.1252-157_1252-155delinsCAA
NM_001270448.2:c.955-157_955-155delinsCAA	NP_001257377.1:n.955-157_955-155delinsCAA