Canonical Allele Identifier: CA497620610

Gene: ACADVL

Linked Data

• ClinVar Variation Id: 1116172
• ClinVar RCV Id: RCV001444477
• dbSNP Id: rs774273664
• gnomAD v3: 17-7223144-C-A
• gnomAD v4: 17-7223144-C-A
• MyVariant Identifiers: chr17:g.7126463C>A (hg19) ; chr17:g.7223144C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7223144C>A , CM000679.2:g.7223144C>A	GRCh38
NC_000017.10:g.7126463C>A , CM000679.1:g.7126463C>A	GRCh37
NC_000017.9:g.7067187C>A	NCBI36
NG_007975.1:g.8311C>A
NG_008391.2:g.1907G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1089C>A MANE Select	ENSP00000349297.5:p.Ala363=
ENST00000322910.9:c.*1044C>A	ENSP00000325395.5:n.*1044C>A
ENST00000350303.9:c.1023C>A	ENSP00000344152.5:p.Ala341=
ENST00000356839.9:c.1089C>A	ENSP00000349297.5:p.Ala363=
ENST00000543245.6:c.1158C>A	ENSP00000438689.2:p.Ala386=
ENST00000578579.2:n.38C>A
ENST00000578824.5:n.505C>A
ENST00000579425.5:n.113C>A
ENST00000582379.1:n.740C>A
ENST00000583858.5:c.118C>A
ENST00000585203.6:n.297C>A
NM_000018.3:c.1089C>A	NP_000009.1:p.Ala363=
NM_001033859.2:c.1023C>A	NP_001029031.1:p.Ala341=
NM_001270447.1:c.1158C>A	NP_001257376.1:p.Ala386=
NM_001270448.1:c.861C>A	NP_001257377.1:p.Ala287=
XM_006721516.2:c.1089C>A	XP_006721579.2:p.Ala363=
XM_011523829.1:c.1089C>A	XP_011522131.1:p.Ala363=
XM_011523830.1:c.1089C>A	XP_011522132.1:p.Ala363=
XR_934021.1:n.1196C>A
XR_934022.1:n.1196C>A
XR_934023.1:n.1196C>A
XM_006721516.3:c.1089C>A	XP_006721579.2:p.Ala363=
XM_011523829.2:c.1089C>A	XP_011522131.1:p.Ala363=
XM_011523830.2:c.1089C>A	XP_011522132.1:p.Ala363=
XM_024450741.1:c.1089C>A	XP_024306509.1:p.Ala363=
XR_934021.2:n.1148C>A
XR_934022.2:n.1148C>A
XR_934023.2:n.1148C>A
NM_000018.4:c.1089C>A MANE Select	NP_000009.1:p.Ala363=
NM_001033859.3:c.1023C>A	NP_001029031.1:p.Ala341=
NM_001270447.2:c.1158C>A	NP_001257376.1:p.Ala386=
NM_001270448.2:c.861C>A	NP_001257377.1:p.Ala287=