Canonical Allele Identifier: CA397724478

Gene: ACADVL

Linked Data

• ClinVar Variation Id: 852414
• ClinVar RCV Id: RCV001057012
• dbSNP Id: rs1422904205
• gnomAD v2: 17-7126533-G-C
• gnomAD v4: 17-7223214-G-C
• MyVariant Identifiers: chr17:g.7126533G>C (hg19) ; chr17:g.7223214G>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1159G>C MANE Select	ENSP00000349297.5:p.Val387Leu
ENST00000322910.9:c.*1114G>C	ENSP00000325395.5:n.*1114G>C
ENST00000350303.9:c.1093G>C	ENSP00000344152.5:p.Val365Leu
ENST00000356839.9:c.1159G>C	ENSP00000349297.5:p.Val387Leu
ENST00000542255.6:c.17G>C
ENST00000543245.6:c.1228G>C	ENSP00000438689.2:p.Val410Leu
ENST00000578579.2:n.108G>C
ENST00000578824.5:n.575G>C
ENST00000579425.5:n.183G>C
ENST00000582379.1:n.810G>C
ENST00000583858.5:c.188G>C
ENST00000585203.6:n.367G>C
NM_000018.3:c.1159G>C	NP_000009.1:p.Val387Leu
NM_001033859.2:c.1093G>C	NP_001029031.1:p.Val365Leu
NM_001270447.1:c.1228G>C	NP_001257376.1:p.Val410Leu
NM_001270448.1:c.931G>C	NP_001257377.1:p.Val311Leu
XM_006721516.2:c.1159G>C	XP_006721579.2:p.Val387Leu
XM_011523829.1:c.1159G>C	XP_011522131.1:p.Val387Leu
XM_011523830.1:c.1159G>C	XP_011522132.1:p.Val387Leu
XR_934021.1:n.1266G>C
XR_934022.1:n.1266G>C
XR_934023.1:n.1266G>C
XM_006721516.3:c.1159G>C	XP_006721579.2:p.Val387Leu
XM_011523829.2:c.1159G>C	XP_011522131.1:p.Val387Leu
XM_011523830.2:c.1159G>C	XP_011522132.1:p.Val387Leu
XM_024450741.1:c.1159G>C	XP_024306509.1:p.Val387Leu
XR_934021.2:n.1218G>C
XR_934022.2:n.1218G>C
XR_934023.2:n.1218G>C
NM_000018.4:c.1159G>C MANE Select	NP_000009.1:p.Val387Leu
NM_001033859.3:c.1093G>C	NP_001029031.1:p.Val365Leu
NM_001270447.2:c.1228G>C	NP_001257376.1:p.Val410Leu
NM_001270448.2:c.931G>C	NP_001257377.1:p.Val311Leu