Canonical Allele Identifier: CA397726137

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7128349T>A (hg19) ; chr17:g.7225030T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7225030T>A , CM000679.2:g.7225030T>A	GRCh38
NC_000017.10:g.7128349T>A , CM000679.1:g.7128349T>A	GRCh37
NC_000017.9:g.7069073T>A	NCBI36
NG_007975.1:g.10197T>A
NG_008391.2:g.21A>T
NG_033038.1:g.14515A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1901T>A MANE Select	ENSP00000349297.5:p.Phe634Tyr
ENST00000322910.9:c.*1856T>A	ENSP00000325395.5:n.*1856T>A
ENST00000350303.9:c.1835T>A	ENSP00000344152.5:p.Phe612Tyr
ENST00000356839.9:c.1901T>A	ENSP00000349297.5:p.Phe634Tyr
ENST00000542255.6:c.780T>A
ENST00000543245.6:c.1970T>A	ENSP00000438689.2:p.Phe657Tyr
ENST00000578033.1:n.326T>A
ENST00000578319.5:n.482T>A
ENST00000578711.1:n.1526T>A
ENST00000578809.5:n.473T>A
ENST00000579425.5:n.1017T>A
ENST00000583848.5:c.267T>A	ENSP00000466487.1:n.267T>A
ENST00000583850.5:n.672T>A
ENST00000583858.5:c.832T>A
NM_000018.3:c.1901T>A	NP_000009.1:p.Phe634Tyr
NM_001033859.2:c.1835T>A	NP_001029031.1:p.Phe612Tyr
NM_001270447.1:c.1970T>A	NP_001257376.1:p.Phe657Tyr
NM_001270448.1:c.1673T>A	NP_001257377.1:p.Phe558Tyr
XM_006721516.2:c.1922T>A	XP_006721579.2:p.Phe641Tyr
XM_011523829.1:c.1820T>A	XP_011522131.1:p.Phe607Tyr
XM_011523830.1:c.1799T>A	XP_011522132.1:p.Phe600Tyr
XR_934021.1:n.2004T>A
XR_934022.1:n.1910T>A
XR_934023.1:n.1931T>A
XM_006721516.3:c.1922T>A	XP_006721579.2:p.Phe641Tyr
XM_011523829.2:c.1820T>A	XP_011522131.1:p.Phe607Tyr
XM_011523830.2:c.1799T>A	XP_011522132.1:p.Phe600Tyr
XM_024450741.1:c.1889T>A	XP_024306509.1:p.Phe630Tyr
XR_934021.2:n.1956T>A
XR_934022.2:n.1862T>A
XR_934023.2:n.1883T>A
NM_000018.4:c.1901T>A MANE Select	NP_000009.1:p.Phe634Tyr
NM_001033859.3:c.1835T>A	NP_001029031.1:p.Phe612Tyr
NM_001270447.2:c.1970T>A	NP_001257376.1:p.Phe657Tyr
NM_001270448.2:c.1673T>A	NP_001257377.1:p.Phe558Tyr