Canonical Allele Identifier: CA397724550

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7126967T>G (hg19) ; chr17:g.7223648T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7223648T>G , CM000679.2:g.7223648T>G	GRCh38
NC_000017.10:g.7126967T>G , CM000679.1:g.7126967T>G	GRCh37
NC_000017.9:g.7067691T>G	NCBI36
NG_007975.1:g.8815T>G
NG_008391.2:g.1403A>C
NG_033038.1:g.15897A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1187T>G MANE Select	ENSP00000349297.5:p.Met396Arg
ENST00000322910.9:c.*1142T>G	ENSP00000325395.5:n.*1142T>G
ENST00000350303.9:c.1121T>G	ENSP00000344152.5:p.Met374Arg
ENST00000356839.9:c.1187T>G	ENSP00000349297.5:p.Met396Arg
ENST00000542255.6:c.45T>G
ENST00000543245.6:c.1256T>G	ENSP00000438689.2:p.Met419Arg
ENST00000578579.2:n.358T>G
ENST00000578711.1:n.144T>G
ENST00000578824.5:n.603T>G
ENST00000579425.5:n.211T>G
ENST00000579546.1:c.24T>G
ENST00000583858.5:c.216T>G
ENST00000585203.6:n.395T>G
NM_000018.3:c.1187T>G	NP_000009.1:p.Met396Arg
NM_001033859.2:c.1121T>G	NP_001029031.1:p.Met374Arg
NM_001270447.1:c.1256T>G	NP_001257376.1:p.Met419Arg
NM_001270448.1:c.959T>G	NP_001257377.1:p.Met320Arg
XM_006721516.2:c.1187T>G	XP_006721579.2:p.Met396Arg
XM_011523829.1:c.1187T>G	XP_011522131.1:p.Met396Arg
XM_011523830.1:c.1187T>G	XP_011522132.1:p.Met396Arg
XR_934021.1:n.1294T>G
XR_934022.1:n.1294T>G
XR_934023.1:n.1294T>G
XM_006721516.3:c.1187T>G	XP_006721579.2:p.Met396Arg
XM_011523829.2:c.1187T>G	XP_011522131.1:p.Met396Arg
XM_011523830.2:c.1187T>G	XP_011522132.1:p.Met396Arg
XM_024450741.1:c.1187T>G	XP_024306509.1:p.Met396Arg
XR_934021.2:n.1246T>G
XR_934022.2:n.1246T>G
XR_934023.2:n.1246T>G
NM_000018.4:c.1187T>G MANE Select	NP_000009.1:p.Met396Arg
NM_001033859.3:c.1121T>G	NP_001029031.1:p.Met374Arg
NM_001270447.2:c.1256T>G	NP_001257376.1:p.Met419Arg
NM_001270448.2:c.959T>G	NP_001257377.1:p.Met320Arg