Canonical Allele Identifier: CA8337686

Gene: ACADVL

Linked Data

• ClinVar Variation Id: 1159893
• ClinVar RCV Id: RCV001503817
• dbSNP Id: rs768219726
• ExAC: 17:7124263 G / A
• gnomAD v2: 17-7124263-G-A
• gnomAD v4: 17-7220944-G-A
• MyVariant Identifiers: chr17:g.7124263G>A (hg19) ; chr17:g.7220944G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7220944G>A , CM000679.2:g.7220944G>A	GRCh38
NC_000017.10:g.7124263G>A , CM000679.1:g.7124263G>A	GRCh37
NC_000017.9:g.7064987G>A	NCBI36
NG_007975.1:g.6111G>A
NG_008391.2:g.4107C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.363G>A MANE Select	ENSP00000349297.5:p.Lys121=
ENST00000322910.9:c.*318G>A	ENSP00000325395.5:n.*318G>A
ENST00000350303.9:c.297G>A	ENSP00000344152.5:p.Lys99=
ENST00000356839.9:c.363G>A	ENSP00000349297.5:p.Lys121=
ENST00000543245.6:c.432G>A	ENSP00000438689.2:p.Lys144=
ENST00000577191.5:n.440G>A
ENST00000577433.5:n.571G>A
ENST00000577857.5:n.293+114G>A
ENST00000579286.5:n.544G>A
ENST00000579886.2:c.202-1G>A	ENSP00000463246.1:n.202-1G>A
ENST00000580365.1:n.94G>A
ENST00000581378.5:c.62G>A
ENST00000581562.5:n.410G>A
ENST00000582056.5:n.546G>A
ENST00000582166.1:n.344G>A
ENST00000583312.5:c.363G>A	ENSP00000467920.1:p.Lys121=
ENST00000584103.5:c.396G>A	ENSP00000465353.1:p.Lys132=
NM_000018.3:c.363G>A	NP_000009.1:p.Lys121=
NM_001033859.2:c.297G>A	NP_001029031.1:p.Lys99=
NM_001270447.1:c.432G>A	NP_001257376.1:p.Lys144=
NM_001270448.1:c.135G>A	NP_001257377.1:p.Lys45=
XM_006721516.2:c.363G>A	XP_006721579.2:p.Lys121=
XM_011523829.1:c.363G>A	XP_011522131.1:p.Lys121=
XM_011523830.1:c.363G>A	XP_011522132.1:p.Lys121=
XR_934021.1:n.470G>A
XR_934022.1:n.470G>A
XR_934023.1:n.470G>A
XM_006721516.3:c.363G>A	XP_006721579.2:p.Lys121=
XM_011523829.2:c.363G>A	XP_011522131.1:p.Lys121=
XM_011523830.2:c.363G>A	XP_011522132.1:p.Lys121=
XM_024450741.1:c.363G>A	XP_024306509.1:p.Lys121=
XR_934021.2:n.422G>A
XR_934022.2:n.422G>A
XR_934023.2:n.422G>A
NM_000018.4:c.363G>A MANE Select	NP_000009.1:p.Lys121=
NM_001033859.3:c.297G>A	NP_001029031.1:p.Lys99=
NM_001270447.2:c.432G>A	NP_001257376.1:p.Lys144=
NM_001270448.2:c.135G>A	NP_001257377.1:p.Lys45=