Canonical Allele Identifier: CA397721939

Gene: ACADVL DLG4

Linked Data

• MyVariant Identifiers: chr17:g.7123328A>C (hg19) ; chr17:g.7220009A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7220009A>C , CM000679.2:g.7220009A>C	GRCh38
NC_000017.10:g.7123328A>C , CM000679.1:g.7123328A>C	GRCh37
NC_000017.9:g.7064052A>C	NCBI36
NG_007975.1:g.5176A>C
NG_008391.2:g.5042T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.25A>C (ACADVL) MANE Select	ENSP00000349297.5:p.Ser9Arg
ENST00000322910.9:c.25A>C (ACADVL)	ENSP00000325395.5:p.Ser9Arg
ENST00000350303.9:c.25A>C (ACADVL)	ENSP00000344152.5:p.Ser9Arg
ENST00000356839.9:c.25A>C (ACADVL)	ENSP00000349297.5:p.Ser9Arg
ENST00000543245.6:c.132-113A>C (ACADVL)	ENSP00000438689.2:n.132-113A>C
ENST00000577191.5:n.102A>C (ACADVL)
ENST00000577857.5:n.115A>C (ACADVL)
ENST00000578269.5:n.132A>C (ACADVL)
ENST00000578421.1:n.84A>C (ACADVL)
ENST00000579286.5:n.132A>C (ACADVL)
ENST00000579886.2:c.25A>C (ACADVL)	ENSP00000463246.1:p.Ser9Arg
ENST00000580263.5:n.115A>C (ACADVL)
ENST00000581562.5:n.72A>C (ACADVL)
ENST00000582056.5:n.115A>C (ACADVL)
ENST00000582356.5:n.150A>C (ACADVL)
ENST00000583312.5:c.25A>C (ACADVL)	ENSP00000467920.1:p.Ser9Arg
ENST00000584103.5:c.25A>C (ACADVL)	ENSP00000465353.1:p.Ser9Arg
NM_000018.3:c.25A>C (ACADVL)	NP_000009.1:p.Ser9Arg
NM_001033859.2:c.25A>C (ACADVL)	NP_001029031.1:p.Ser9Arg
NM_001270447.1:c.132-113A>C (ACADVL)	NP_001257376.1:n.132-113A>C
NM_001270448.1:c.-279A>C (ACADVL)	NP_001257377.1:n.-279A>C
NM_001365.3:c.-1160T>G (DLG4)	NP_001356.1:n.-1160T>G
XM_006721516.2:c.25A>C (ACADVL)	XP_006721579.2:p.Ser9Arg
XM_011523829.1:c.25A>C (ACADVL)	XP_011522131.1:p.Ser9Arg
XM_011523830.1:c.25A>C (ACADVL)	XP_011522132.1:p.Ser9Arg
XR_934021.1:n.132A>C (ACADVL)
XR_934022.1:n.132A>C (ACADVL)
XR_934023.1:n.132A>C (ACADVL)
NM_001321074.1:c.-1160T>G (DLG4)	NP_001308003.1:n.-1160T>G
NM_001365.4:c.-1160T>G (DLG4)	NP_001356.1:n.-1160T>G
NR_135527.1:n.42T>G (DLG4)
XM_006721516.3:c.25A>C (ACADVL)	XP_006721579.2:p.Ser9Arg
XM_011523829.2:c.25A>C (ACADVL)	XP_011522131.1:p.Ser9Arg
XM_011523830.2:c.25A>C (ACADVL)	XP_011522132.1:p.Ser9Arg
XM_024450741.1:c.25A>C (ACADVL)	XP_024306509.1:p.Ser9Arg
XR_934021.2:n.84A>C (ACADVL)
XR_934022.2:n.84A>C (ACADVL)
XR_934023.2:n.84A>C (ACADVL)
NM_000018.4:c.25A>C (ACADVL) MANE Select	NP_000009.1:p.Ser9Arg
NM_001033859.3:c.25A>C (ACADVL)	NP_001029031.1:p.Ser9Arg
NM_001270447.2:c.132-113A>C (ACADVL)	NP_001257376.1:n.132-113A>C
NM_001270448.2:c.-279A>C (ACADVL)	NP_001257377.1:n.-279A>C