Canonical Allele Identifier: CA497621530

Gene: ACADVL MIR324

Linked Data

• MyVariant Identifiers: chr17:g.7126689G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7223370G>C , CM000679.2:g.7223370G>C	GRCh38
NC_000017.10:g.7126689G>C , CM000679.1:g.7126689G>C	GRCh37
NC_000017.9:g.7067413G>C	NCBI36
NG_007975.1:g.8537G>C
NG_008391.2:g.1681C>G
NG_033038.1:g.16175C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1182+133G>C (ACADVL) MANE Select	ENSP00000349297.5:n.1182+133G>C
ENST00000322910.9:c.*1137+133G>C (ACADVL)	ENSP00000325395.5:n.*1137+133G>C
ENST00000350303.9:c.1116+133G>C (ACADVL)	ENSP00000344152.5:n.1116+133G>C
ENST00000356839.9:c.1182+133G>C (ACADVL)	ENSP00000349297.5:n.1182+133G>C
ENST00000542255.6:c.40+133G>C (ACADVL)
ENST00000543245.6:c.1251+133G>C (ACADVL)	ENSP00000438689.2:n.1251+133G>C
ENST00000578579.2:n.132-52G>C (ACADVL)
ENST00000578824.5:n.598+133G>C (ACADVL)
ENST00000579425.5:n.206+133G>C (ACADVL)
ENST00000579546.1:c.19+133G>C (ACADVL)
ENST00000583858.5:c.211+133G>C (ACADVL)
ENST00000585203.6:n.390+133G>C (ACADVL)
NM_000018.3:c.1182+133G>C (ACADVL)	NP_000009.1:n.1182+133G>C
NM_001033859.2:c.1116+133G>C (ACADVL)	NP_001029031.1:n.1116+133G>C
NM_001270447.1:c.1251+133G>C (ACADVL)	NP_001257376.1:n.1251+133G>C
NM_001270448.1:c.954+133G>C (ACADVL)	NP_001257377.1:n.954+133G>C
NR_029896.1:n.10C>G (MIR324)
XM_006721516.2:c.1182+133G>C (ACADVL)	XP_006721579.2:n.1182+133G>C
XM_011523829.1:c.1182+133G>C (ACADVL)	XP_011522131.1:n.1182+133G>C
XM_011523830.1:c.1182+133G>C (ACADVL)	XP_011522132.1:n.1182+133G>C
XR_934021.1:n.1289+133G>C (ACADVL)
XR_934022.1:n.1289+133G>C (ACADVL)
XR_934023.1:n.1289+133G>C (ACADVL)
XM_006721516.3:c.1182+133G>C (ACADVL)	XP_006721579.2:n.1182+133G>C
XM_011523829.2:c.1182+133G>C (ACADVL)	XP_011522131.1:n.1182+133G>C
XM_011523830.2:c.1182+133G>C (ACADVL)	XP_011522132.1:n.1182+133G>C
XM_024450741.1:c.1182+133G>C (ACADVL)	XP_024306509.1:n.1182+133G>C
XR_934021.2:n.1241+133G>C (ACADVL)
XR_934022.2:n.1241+133G>C (ACADVL)
XR_934023.2:n.1241+133G>C (ACADVL)
NM_000018.4:c.1182+133G>C (ACADVL) MANE Select	NP_000009.1:n.1182+133G>C
NM_001033859.3:c.1116+133G>C (ACADVL)	NP_001029031.1:n.1116+133G>C
NM_001270447.2:c.1251+133G>C (ACADVL)	NP_001257376.1:n.1251+133G>C
NM_001270448.2:c.954+133G>C (ACADVL)	NP_001257377.1:n.954+133G>C