Canonical Allele Identifier: CA397722795

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7124286A>T (hg19) ; chr17:g.7220967A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7220967A>T , CM000679.2:g.7220967A>T	GRCh38
NC_000017.10:g.7124286A>T , CM000679.1:g.7124286A>T	GRCh37
NC_000017.9:g.7065010A>T	NCBI36
NG_007975.1:g.6134A>T
NG_008391.2:g.4084T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.386A>T MANE Select	ENSP00000349297.5:p.Glu129Val
ENST00000322910.9:c.*341A>T	ENSP00000325395.5:n.*341A>T
ENST00000350303.9:c.320A>T	ENSP00000344152.5:p.Glu107Val
ENST00000356839.9:c.386A>T	ENSP00000349297.5:p.Glu129Val
ENST00000543245.6:c.455A>T	ENSP00000438689.2:p.Glu152Val
ENST00000577191.5:n.463A>T
ENST00000577433.5:n.594A>T
ENST00000577857.5:n.293+137A>T
ENST00000579286.5:n.567A>T
ENST00000579886.2:c.224A>T	ENSP00000463246.1:p.Glu75Val
ENST00000580365.1:n.117A>T
ENST00000581378.5:c.85A>T
ENST00000581562.5:n.433A>T
ENST00000582056.5:n.569A>T
ENST00000582166.1:n.367A>T
ENST00000583312.5:c.386A>T	ENSP00000467920.1:p.Glu129Val
ENST00000584103.5:c.419A>T	ENSP00000465353.1:p.Glu140Val
NM_000018.3:c.386A>T	NP_000009.1:p.Glu129Val
NM_001033859.2:c.320A>T	NP_001029031.1:p.Glu107Val
NM_001270447.1:c.455A>T	NP_001257376.1:p.Glu152Val
NM_001270448.1:c.158A>T	NP_001257377.1:p.Glu53Val
XM_006721516.2:c.386A>T	XP_006721579.2:p.Glu129Val
XM_011523829.1:c.386A>T	XP_011522131.1:p.Glu129Val
XM_011523830.1:c.386A>T	XP_011522132.1:p.Glu129Val
XR_934021.1:n.493A>T
XR_934022.1:n.493A>T
XR_934023.1:n.493A>T
XM_006721516.3:c.386A>T	XP_006721579.2:p.Glu129Val
XM_011523829.2:c.386A>T	XP_011522131.1:p.Glu129Val
XM_011523830.2:c.386A>T	XP_011522132.1:p.Glu129Val
XM_024450741.1:c.386A>T	XP_024306509.1:p.Glu129Val
XR_934021.2:n.445A>T
XR_934022.2:n.445A>T
XR_934023.2:n.445A>T
NM_000018.4:c.386A>T MANE Select	NP_000009.1:p.Glu129Val
NM_001033859.3:c.320A>T	NP_001029031.1:p.Glu107Val
NM_001270447.2:c.455A>T	NP_001257376.1:p.Glu152Val
NM_001270448.2:c.158A>T	NP_001257377.1:p.Glu53Val