Canonical Allele Identifier: CA397724477

Gene: ACADVL

Linked Data

• ClinVar Variation Id: 1345350
• ClinVar RCV Id: RCV002049825
• dbSNP Id: rs1422904205
• gnomAD v2: 17-7126533-G-A
• gnomAD v3: 17-7223214-G-A
• gnomAD v4: 17-7223214-G-A
• MyVariant Identifiers: chr17:g.7126533G>A (hg19) ; chr17:g.7223214G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7223214G>A , CM000679.2:g.7223214G>A	GRCh38
NC_000017.10:g.7126533G>A , CM000679.1:g.7126533G>A	GRCh37
NC_000017.9:g.7067257G>A	NCBI36
NG_007975.1:g.8381G>A
NG_008391.2:g.1837C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1159G>A MANE Select	ENSP00000349297.5:p.Val387Ile
ENST00000322910.9:c.*1114G>A	ENSP00000325395.5:n.*1114G>A
ENST00000350303.9:c.1093G>A	ENSP00000344152.5:p.Val365Ile
ENST00000356839.9:c.1159G>A	ENSP00000349297.5:p.Val387Ile
ENST00000542255.6:c.17G>A
ENST00000543245.6:c.1228G>A	ENSP00000438689.2:p.Val410Ile
ENST00000578579.2:n.108G>A
ENST00000578824.5:n.575G>A
ENST00000579425.5:n.183G>A
ENST00000582379.1:n.810G>A
ENST00000583858.5:c.188G>A
ENST00000585203.6:n.367G>A
NM_000018.3:c.1159G>A	NP_000009.1:p.Val387Ile
NM_001033859.2:c.1093G>A	NP_001029031.1:p.Val365Ile
NM_001270447.1:c.1228G>A	NP_001257376.1:p.Val410Ile
NM_001270448.1:c.931G>A	NP_001257377.1:p.Val311Ile
XM_006721516.2:c.1159G>A	XP_006721579.2:p.Val387Ile
XM_011523829.1:c.1159G>A	XP_011522131.1:p.Val387Ile
XM_011523830.1:c.1159G>A	XP_011522132.1:p.Val387Ile
XR_934021.1:n.1266G>A
XR_934022.1:n.1266G>A
XR_934023.1:n.1266G>A
XM_006721516.3:c.1159G>A	XP_006721579.2:p.Val387Ile
XM_011523829.2:c.1159G>A	XP_011522131.1:p.Val387Ile
XM_011523830.2:c.1159G>A	XP_011522132.1:p.Val387Ile
XM_024450741.1:c.1159G>A	XP_024306509.1:p.Val387Ile
XR_934021.2:n.1218G>A
XR_934022.2:n.1218G>A
XR_934023.2:n.1218G>A
NM_000018.4:c.1159G>A MANE Select	NP_000009.1:p.Val387Ile
NM_001033859.3:c.1093G>A	NP_001029031.1:p.Val365Ile
NM_001270447.2:c.1228G>A	NP_001257376.1:p.Val410Ile
NM_001270448.2:c.931G>A	NP_001257377.1:p.Val311Ile