Canonical Allele Identifier: CA397722542

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7124110T>A (hg19) ; chr17:g.7220791T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7220791T>A , CM000679.2:g.7220791T>A	GRCh38
NC_000017.10:g.7124110T>A , CM000679.1:g.7124110T>A	GRCh37
NC_000017.9:g.7064834T>A	NCBI36
NG_007975.1:g.5958T>A
NG_008391.2:g.4260A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.303T>A MANE Select	ENSP00000349297.5:p.Phe101Leu
ENST00000322910.9:c.*258T>A	ENSP00000325395.5:n.*258T>A
ENST00000350303.9:c.237T>A	ENSP00000344152.5:p.Phe79Leu
ENST00000356839.9:c.303T>A	ENSP00000349297.5:p.Phe101Leu
ENST00000543245.6:c.372T>A	ENSP00000438689.2:p.Phe124Leu
ENST00000577191.5:n.380T>A
ENST00000577433.5:n.511T>A
ENST00000577857.5:n.254T>A
ENST00000579286.5:n.484T>A
ENST00000579886.2:c.202-154T>A	ENSP00000463246.1:n.202-154T>A
ENST00000580365.1:n.34T>A
ENST00000581378.5:c.2T>A
ENST00000581562.5:n.350T>A
ENST00000582056.5:n.393T>A
ENST00000582166.1:n.191T>A
ENST00000582356.5:n.502T>A
ENST00000583312.5:c.303T>A	ENSP00000467920.1:p.Phe101Leu
ENST00000584103.5:c.303T>A	ENSP00000465353.1:p.Phe101Leu
NM_000018.3:c.303T>A	NP_000009.1:p.Phe101Leu
NM_001033859.2:c.237T>A	NP_001029031.1:p.Phe79Leu
NM_001270447.1:c.372T>A	NP_001257376.1:p.Phe124Leu
NM_001270448.1:c.75T>A	NP_001257377.1:p.Phe25Leu
XM_006721516.2:c.303T>A	XP_006721579.2:p.Phe101Leu
XM_011523829.1:c.303T>A	XP_011522131.1:p.Phe101Leu
XM_011523830.1:c.303T>A	XP_011522132.1:p.Phe101Leu
XR_934021.1:n.410T>A
XR_934022.1:n.410T>A
XR_934023.1:n.410T>A
XM_006721516.3:c.303T>A	XP_006721579.2:p.Phe101Leu
XM_011523829.2:c.303T>A	XP_011522131.1:p.Phe101Leu
XM_011523830.2:c.303T>A	XP_011522132.1:p.Phe101Leu
XM_024450741.1:c.303T>A	XP_024306509.1:p.Phe101Leu
XR_934021.2:n.362T>A
XR_934022.2:n.362T>A
XR_934023.2:n.362T>A
NM_000018.4:c.303T>A MANE Select	NP_000009.1:p.Phe101Leu
NM_001033859.3:c.237T>A	NP_001029031.1:p.Phe79Leu
NM_001270447.2:c.372T>A	NP_001257376.1:p.Phe124Leu
NM_001270448.2:c.75T>A	NP_001257377.1:p.Phe25Leu