Canonical Allele Identifier: CA397724998

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7127337T>G (hg19) ; chr17:g.7224018T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224018T>G , CM000679.2:g.7224018T>G	GRCh38
NC_000017.10:g.7127337T>G , CM000679.1:g.7127337T>G	GRCh37
NC_000017.9:g.7068061T>G	NCBI36
NG_007975.1:g.9185T>G
NG_008391.2:g.1033A>C
NG_033038.1:g.15527A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.1383T>G MANE Select	ENSP00000349297.5:p.Phe461Leu
ENST00000322910.9:c.*1338T>G	ENSP00000325395.5:n.*1338T>G
ENST00000350303.9:c.1317T>G	ENSP00000344152.5:p.Phe439Leu
ENST00000356839.9:c.1383T>G	ENSP00000349297.5:p.Phe461Leu
ENST00000542255.6:c.241T>G
ENST00000543245.6:c.1452T>G	ENSP00000438689.2:p.Phe484Leu
ENST00000578711.1:n.514T>G
ENST00000579425.5:n.499T>G
ENST00000579546.1:c.220T>G
ENST00000579894.5:n.94T>G
ENST00000583074.5:n.102T>G
ENST00000583850.5:n.158T>G
ENST00000583858.5:c.412T>G
ENST00000585203.6:n.574T>G
NM_000018.3:c.1383T>G	NP_000009.1:p.Phe461Leu
NM_001033859.2:c.1317T>G	NP_001029031.1:p.Phe439Leu
NM_001270447.1:c.1452T>G	NP_001257376.1:p.Phe484Leu
NM_001270448.1:c.1155T>G	NP_001257377.1:p.Phe385Leu
XM_006721516.2:c.1383T>G	XP_006721579.2:p.Phe461Leu
XM_011523829.1:c.1383T>G	XP_011522131.1:p.Phe461Leu
XM_011523830.1:c.1383T>G	XP_011522132.1:p.Phe461Leu
XR_934021.1:n.1490T>G
XR_934022.1:n.1490T>G
XR_934023.1:n.1490T>G
XM_006721516.3:c.1383T>G	XP_006721579.2:p.Phe461Leu
XM_011523829.2:c.1383T>G	XP_011522131.1:p.Phe461Leu
XM_011523830.2:c.1383T>G	XP_011522132.1:p.Phe461Leu
XM_024450741.1:c.1383T>G	XP_024306509.1:p.Phe461Leu
XR_934021.2:n.1442T>G
XR_934022.2:n.1442T>G
XR_934023.2:n.1442T>G
NM_000018.4:c.1383T>G MANE Select	NP_000009.1:p.Phe461Leu
NM_001033859.3:c.1317T>G	NP_001029031.1:p.Phe439Leu
NM_001270447.2:c.1452T>G	NP_001257376.1:p.Phe484Leu
NM_001270448.2:c.1155T>G	NP_001257377.1:p.Phe385Leu