Canonical Allele Identifier: CA8337617

Gene: ACADVL

Linked Data

• ClinVar Variation Id: 2172652
• ClinVar RCV Id: RCV003097652
• dbSNP Id: rs768632138
• ExAC: 17:7123995 G / A
• gnomAD v2: 17-7123995-G-A
• gnomAD v3: 17-7220676-G-A
• gnomAD v4: 17-7220676-G-A
• MyVariant Identifiers: chr17:g.7123995G>A (hg19) ; chr17:g.7220676G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7220676G>A , CM000679.2:g.7220676G>A	GRCh38
NC_000017.10:g.7123995G>A , CM000679.1:g.7123995G>A	GRCh37
NC_000017.9:g.7064719G>A	NCBI36
NG_007975.1:g.5843G>A
NG_008391.2:g.4375C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.277G>A MANE Select	ENSP00000349297.5:p.Val93Met
ENST00000322910.9:c.*232G>A	ENSP00000325395.5:n.*232G>A
ENST00000350303.9:c.211G>A	ENSP00000344152.5:p.Val71Met
ENST00000356839.9:c.277G>A	ENSP00000349297.5:p.Val93Met
ENST00000543245.6:c.346G>A	ENSP00000438689.2:p.Val116Met
ENST00000577191.5:n.354G>A
ENST00000577433.5:n.485G>A
ENST00000577857.5:n.229-90G>A
ENST00000578269.5:n.724G>A
ENST00000578421.1:n.485G>A
ENST00000579286.5:n.458G>A
ENST00000579886.2:c.201+150G>A	ENSP00000463246.1:n.201+150G>A
ENST00000580263.5:n.441G>A
ENST00000581562.5:n.324G>A
ENST00000582056.5:n.367G>A
ENST00000582166.1:n.165G>A
ENST00000582356.5:n.476G>A
ENST00000583312.5:c.277G>A	ENSP00000467920.1:p.Val93Met
ENST00000584103.5:c.277G>A	ENSP00000465353.1:p.Val93Met
NM_000018.3:c.277G>A	NP_000009.1:p.Val93Met
NM_001033859.2:c.211G>A	NP_001029031.1:p.Val71Met
NM_001270447.1:c.346G>A	NP_001257376.1:p.Val116Met
NM_001270448.1:c.49G>A	NP_001257377.1:p.Val17Met
XM_006721516.2:c.277G>A	XP_006721579.2:p.Val93Met
XM_011523829.1:c.277G>A	XP_011522131.1:p.Val93Met
XM_011523830.1:c.277G>A	XP_011522132.1:p.Val93Met
XR_934021.1:n.384G>A
XR_934022.1:n.384G>A
XR_934023.1:n.384G>A
XM_006721516.3:c.277G>A	XP_006721579.2:p.Val93Met
XM_011523829.2:c.277G>A	XP_011522131.1:p.Val93Met
XM_011523830.2:c.277G>A	XP_011522132.1:p.Val93Met
XM_024450741.1:c.277G>A	XP_024306509.1:p.Val93Met
XR_934021.2:n.336G>A
XR_934022.2:n.336G>A
XR_934023.2:n.336G>A
NM_000018.4:c.277G>A MANE Select	NP_000009.1:p.Val93Met
NM_001033859.3:c.211G>A	NP_001029031.1:p.Val71Met
NM_001270447.2:c.346G>A	NP_001257376.1:p.Val116Met
NM_001270448.2:c.49G>A	NP_001257377.1:p.Val17Met