Canonical Allele Identifier: CA397725147

Gene: ACADVL

Linked Data

• gnomAD v4: 17-7224158-G-A
• MyVariant Identifiers: chr17:g.7127477G>A (hg19) ; chr17:g.7224158G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224158G>A , CM000679.2:g.7224158G>A	GRCh38
NC_000017.10:g.7127477G>A , CM000679.1:g.7127477G>A	GRCh37
NC_000017.9:g.7068201G>A	NCBI36
NG_007975.1:g.9325G>A
NG_008391.2:g.893C>T
NG_033038.1:g.15387C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.1447G>A MANE Select	ENSP00000349297.5:p.Glu483Lys
ENST00000322910.9:c.*1402G>A	ENSP00000325395.5:n.*1402G>A
ENST00000350303.9:c.1381G>A	ENSP00000344152.5:p.Glu461Lys
ENST00000356839.9:c.1447G>A	ENSP00000349297.5:p.Glu483Lys
ENST00000542255.6:c.305G>A
ENST00000543245.6:c.1516G>A	ENSP00000438689.2:p.Glu506Lys
ENST00000578711.1:n.654G>A
ENST00000579391.1:n.55G>A
ENST00000579425.5:n.563G>A
ENST00000579546.1:c.271+89G>A
ENST00000579894.5:n.234G>A
ENST00000583074.5:n.153+89G>A
ENST00000583850.5:n.222G>A
ENST00000583858.5:c.463+89G>A
ENST00000585203.6:n.638G>A
NM_000018.3:c.1447G>A	NP_000009.1:p.Glu483Lys
NM_001033859.2:c.1381G>A	NP_001029031.1:p.Glu461Lys
NM_001270447.1:c.1516G>A	NP_001257376.1:p.Glu506Lys
NM_001270448.1:c.1219G>A	NP_001257377.1:p.Glu407Lys
XM_006721516.2:c.1447G>A	XP_006721579.2:p.Glu483Lys
XM_011523829.1:c.1434+89G>A	XP_011522131.1:n.1434+89G>A
XM_011523830.1:c.1434+89G>A	XP_011522132.1:n.1434+89G>A
XR_934021.1:n.1554G>A
XR_934022.1:n.1541+89G>A
XR_934023.1:n.1541+89G>A
XM_006721516.3:c.1447G>A	XP_006721579.2:p.Glu483Lys
XM_011523829.2:c.1434+89G>A	XP_011522131.1:n.1434+89G>A
XM_011523830.2:c.1434+89G>A	XP_011522132.1:n.1434+89G>A
XM_024450741.1:c.1434+89G>A	XP_024306509.1:n.1434+89G>A
XR_934021.2:n.1506G>A
XR_934022.2:n.1493+89G>A
XR_934023.2:n.1493+89G>A
NM_000018.4:c.1447G>A MANE Select	NP_000009.1:p.Glu483Lys
NM_001033859.3:c.1381G>A	NP_001029031.1:p.Glu461Lys
NM_001270447.2:c.1516G>A	NP_001257376.1:p.Glu506Lys
NM_001270448.2:c.1219G>A	NP_001257377.1:p.Glu407Lys