Canonical Allele Identifier: CA2245710905

Gene: ACADVL MIR324

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7223331_7223334delinsTCTC , CM000679.2:g.7223331_7223334delinsTCTC	GRCh38
NC_000017.10:g.7126650_7126653delinsTCTC , CM000679.1:g.7126650_7126653delinsTCTC	GRCh37
NC_000017.9:g.7067374_7067377delinsTCTC	NCBI36
NG_007975.1:g.8498_8501delinsTCTC
NG_008391.2:g.1717_1720delinsGAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1182+94_1182+97delinsTCTC (ACADVL) MANE Select	ENSP00000349297.5:n.1182+94_1182+97delinsTCTC
ENST00000322910.9:c.*1137+94_*1137+97delinsTCTC (ACADVL)	ENSP00000325395.5:n.*1137+94_*1137+97delinsTCTC
ENST00000350303.9:c.1116+94_1116+97delinsTCTC (ACADVL)	ENSP00000344152.5:n.1116+94_1116+97delinsTCTC
ENST00000356839.9:c.1182+94_1182+97delinsTCTC (ACADVL)	ENSP00000349297.5:n.1182+94_1182+97delinsTCTC
ENST00000542255.6:c.40+94_40+97delinsTCTC (ACADVL)
ENST00000543245.6:c.1251+94_1251+97delinsTCTC (ACADVL)	ENSP00000438689.2:n.1251+94_1251+97delinsTCTC
ENST00000578579.2:n.132-91_132-88delinsTCTC (ACADVL)
ENST00000578824.5:n.598+94_598+97delinsTCTC (ACADVL)
ENST00000579425.5:n.206+94_206+97delinsTCTC (ACADVL)
ENST00000579546.1:c.19+94_19+97delinsTCTC (ACADVL)
ENST00000583858.5:c.211+94_211+97delinsTCTC (ACADVL)
ENST00000585203.6:n.390+94_390+97delinsTCTC (ACADVL)
NM_000018.3:c.1182+94_1182+97delinsTCTC (ACADVL)	NP_000009.1:n.1182+94_1182+97delinsTCTC
NM_001033859.2:c.1116+94_1116+97delinsTCTC (ACADVL)	NP_001029031.1:n.1116+94_1116+97delinsTCTC
NM_001270447.1:c.1251+94_1251+97delinsTCTC (ACADVL)	NP_001257376.1:n.1251+94_1251+97delinsTCTC
NM_001270448.1:c.954+94_954+97delinsTCTC (ACADVL)	NP_001257377.1:n.954+94_954+97delinsTCTC
NR_029896.1:n.46_49delinsGAGA (MIR324)
XM_006721516.2:c.1182+94_1182+97delinsTCTC (ACADVL)	XP_006721579.2:n.1182+94_1182+97delinsTCTC
XM_011523829.1:c.1182+94_1182+97delinsTCTC (ACADVL)	XP_011522131.1:n.1182+94_1182+97delinsTCTC
XM_011523830.1:c.1182+94_1182+97delinsTCTC (ACADVL)	XP_011522132.1:n.1182+94_1182+97delinsTCTC
XR_934021.1:n.1289+94_1289+97delinsTCTC (ACADVL)
XR_934022.1:n.1289+94_1289+97delinsTCTC (ACADVL)
XR_934023.1:n.1289+94_1289+97delinsTCTC (ACADVL)
XM_006721516.3:c.1182+94_1182+97delinsTCTC (ACADVL)	XP_006721579.2:n.1182+94_1182+97delinsTCTC
XM_011523829.2:c.1182+94_1182+97delinsTCTC (ACADVL)	XP_011522131.1:n.1182+94_1182+97delinsTCTC
XM_011523830.2:c.1182+94_1182+97delinsTCTC (ACADVL)	XP_011522132.1:n.1182+94_1182+97delinsTCTC
XM_024450741.1:c.1182+94_1182+97delinsTCTC (ACADVL)	XP_024306509.1:n.1182+94_1182+97delinsTCTC
XR_934021.2:n.1241+94_1241+97delinsTCTC (ACADVL)
XR_934022.2:n.1241+94_1241+97delinsTCTC (ACADVL)
XR_934023.2:n.1241+94_1241+97delinsTCTC (ACADVL)
NM_000018.4:c.1182+94_1182+97delinsTCTC (ACADVL) MANE Select	NP_000009.1:n.1182+94_1182+97delinsTCTC
NM_001033859.3:c.1116+94_1116+97delinsTCTC (ACADVL)	NP_001029031.1:n.1116+94_1116+97delinsTCTC
NM_001270447.2:c.1251+94_1251+97delinsTCTC (ACADVL)	NP_001257376.1:n.1251+94_1251+97delinsTCTC
NM_001270448.2:c.954+94_954+97delinsTCTC (ACADVL)	NP_001257377.1:n.954+94_954+97delinsTCTC