Canonical Allele Identifier: CA497621382

Gene: ACADVL MIR324

Linked Data

• MyVariant Identifiers: chr17:g.7126665C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7223346C>G , CM000679.2:g.7223346C>G	GRCh38
NC_000017.10:g.7126665C>G , CM000679.1:g.7126665C>G	GRCh37
NC_000017.9:g.7067389C>G	NCBI36
NG_007975.1:g.8513C>G
NG_008391.2:g.1705G>C
NG_033038.1:g.16199G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1182+109C>G (ACADVL) MANE Select	ENSP00000349297.5:n.1182+109C>G
ENST00000322910.9:c.*1137+109C>G (ACADVL)	ENSP00000325395.5:n.*1137+109C>G
ENST00000350303.9:c.1116+109C>G (ACADVL)	ENSP00000344152.5:n.1116+109C>G
ENST00000356839.9:c.1182+109C>G (ACADVL)	ENSP00000349297.5:n.1182+109C>G
ENST00000542255.6:c.40+109C>G (ACADVL)
ENST00000543245.6:c.1251+109C>G (ACADVL)	ENSP00000438689.2:n.1251+109C>G
ENST00000578579.2:n.132-76C>G (ACADVL)
ENST00000578824.5:n.598+109C>G (ACADVL)
ENST00000579425.5:n.206+109C>G (ACADVL)
ENST00000579546.1:c.19+109C>G (ACADVL)
ENST00000583858.5:c.211+109C>G (ACADVL)
ENST00000585203.6:n.390+109C>G (ACADVL)
NM_000018.3:c.1182+109C>G (ACADVL)	NP_000009.1:n.1182+109C>G
NM_001033859.2:c.1116+109C>G (ACADVL)	NP_001029031.1:n.1116+109C>G
NM_001270447.1:c.1251+109C>G (ACADVL)	NP_001257376.1:n.1251+109C>G
NM_001270448.1:c.954+109C>G (ACADVL)	NP_001257377.1:n.954+109C>G
NR_029896.1:n.34G>C (MIR324)
XM_006721516.2:c.1182+109C>G (ACADVL)	XP_006721579.2:n.1182+109C>G
XM_011523829.1:c.1182+109C>G (ACADVL)	XP_011522131.1:n.1182+109C>G
XM_011523830.1:c.1182+109C>G (ACADVL)	XP_011522132.1:n.1182+109C>G
XR_934021.1:n.1289+109C>G (ACADVL)
XR_934022.1:n.1289+109C>G (ACADVL)
XR_934023.1:n.1289+109C>G (ACADVL)
XM_006721516.3:c.1182+109C>G (ACADVL)	XP_006721579.2:n.1182+109C>G
XM_011523829.2:c.1182+109C>G (ACADVL)	XP_011522131.1:n.1182+109C>G
XM_011523830.2:c.1182+109C>G (ACADVL)	XP_011522132.1:n.1182+109C>G
XM_024450741.1:c.1182+109C>G (ACADVL)	XP_024306509.1:n.1182+109C>G
XR_934021.2:n.1241+109C>G (ACADVL)
XR_934022.2:n.1241+109C>G (ACADVL)
XR_934023.2:n.1241+109C>G (ACADVL)
NM_000018.4:c.1182+109C>G (ACADVL) MANE Select	NP_000009.1:n.1182+109C>G
NM_001033859.3:c.1116+109C>G (ACADVL)	NP_001029031.1:n.1116+109C>G
NM_001270447.2:c.1251+109C>G (ACADVL)	NP_001257376.1:n.1251+109C>G
NM_001270448.2:c.954+109C>G (ACADVL)	NP_001257377.1:n.954+109C>G