Canonical Allele Identifier: CA397721927

Gene: ACADVL DLG4

Linked Data

• MyVariant Identifiers: chr17:g.7123322G>A (hg19) ; chr17:g.7220003G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7220003G>A , CM000679.2:g.7220003G>A	GRCh38
NC_000017.10:g.7123322G>A , CM000679.1:g.7123322G>A	GRCh37
NC_000017.9:g.7064046G>A	NCBI36
NG_007975.1:g.5170G>A
NG_008391.2:g.5048C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.19G>A (ACADVL) MANE Select	ENSP00000349297.5:p.Ala7Thr
ENST00000322910.9:c.19G>A (ACADVL)	ENSP00000325395.5:p.Ala7Thr
ENST00000350303.9:c.19G>A (ACADVL)	ENSP00000344152.5:p.Ala7Thr
ENST00000356839.9:c.19G>A (ACADVL)	ENSP00000349297.5:p.Ala7Thr
ENST00000543245.6:c.132-119G>A (ACADVL)	ENSP00000438689.2:n.132-119G>A
ENST00000577191.5:n.96G>A (ACADVL)
ENST00000577857.5:n.109G>A (ACADVL)
ENST00000578269.5:n.126G>A (ACADVL)
ENST00000578421.1:n.78G>A (ACADVL)
ENST00000579286.5:n.126G>A (ACADVL)
ENST00000579886.2:c.19G>A (ACADVL)	ENSP00000463246.1:p.Ala7Thr
ENST00000580263.5:n.109G>A (ACADVL)
ENST00000581562.5:n.66G>A (ACADVL)
ENST00000582056.5:n.109G>A (ACADVL)
ENST00000582356.5:n.144G>A (ACADVL)
ENST00000583312.5:c.19G>A (ACADVL)	ENSP00000467920.1:p.Ala7Thr
ENST00000584103.5:c.19G>A (ACADVL)	ENSP00000465353.1:p.Ala7Thr
NM_000018.3:c.19G>A (ACADVL)	NP_000009.1:p.Ala7Thr
NM_001033859.2:c.19G>A (ACADVL)	NP_001029031.1:p.Ala7Thr
NM_001270447.1:c.132-119G>A (ACADVL)	NP_001257376.1:n.132-119G>A
NM_001270448.1:c.-285G>A (ACADVL)	NP_001257377.1:n.-285G>A
NM_001365.3:c.-1154C>T (DLG4)	NP_001356.1:n.-1154C>T
XM_006721516.2:c.19G>A (ACADVL)	XP_006721579.2:p.Ala7Thr
XM_011523829.1:c.19G>A (ACADVL)	XP_011522131.1:p.Ala7Thr
XM_011523830.1:c.19G>A (ACADVL)	XP_011522132.1:p.Ala7Thr
XR_934021.1:n.126G>A (ACADVL)
XR_934022.1:n.126G>A (ACADVL)
XR_934023.1:n.126G>A (ACADVL)
NM_001321074.1:c.-1154C>T (DLG4)	NP_001308003.1:n.-1154C>T
NM_001365.4:c.-1154C>T (DLG4)	NP_001356.1:n.-1154C>T
NR_135527.1:n.48C>T (DLG4)
XM_006721516.3:c.19G>A (ACADVL)	XP_006721579.2:p.Ala7Thr
XM_011523829.2:c.19G>A (ACADVL)	XP_011522131.1:p.Ala7Thr
XM_011523830.2:c.19G>A (ACADVL)	XP_011522132.1:p.Ala7Thr
XM_024450741.1:c.19G>A (ACADVL)	XP_024306509.1:p.Ala7Thr
XR_934021.2:n.78G>A (ACADVL)
XR_934022.2:n.78G>A (ACADVL)
XR_934023.2:n.78G>A (ACADVL)
NM_000018.4:c.19G>A (ACADVL) MANE Select	NP_000009.1:p.Ala7Thr
NM_001033859.3:c.19G>A (ACADVL)	NP_001029031.1:p.Ala7Thr
NM_001270447.2:c.132-119G>A (ACADVL)	NP_001257376.1:n.132-119G>A
NM_001270448.2:c.-285G>A (ACADVL)	NP_001257377.1:n.-285G>A