Canonical Allele Identifier: CA497694078
Gene: ACADVL HGNC NCBI

Linked Data

ClinVar Variation Id: 721658
ClinVar RCV Id: RCV001470164
dbSNP Id: rs1597533902
gnomAD v3: 17-7223661-G-A
gnomAD v4: 17-7223661-G-A
MyVariant Identifiers: chr17:g.7126980G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223661G>A , CM000679.2:g.7223661G>A GRCh38
NC_000017.10:g.7126980G>A , CM000679.1:g.7126980G>A GRCh37
NC_000017.9:g.7067704G>A NCBI36
NG_007975.1:g.8828G>A
NG_008391.2:g.1390C>T
NG_033038.1:g.15884C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1200G>A MANE Select ENSP00000349297.5:p.Val400=
ENST00000322910.9:c.*1155G>A ENSP00000325395.5:n.*1155G>A
ENST00000350303.9:c.1134G>A ENSP00000344152.5:p.Val378=
ENST00000356839.9:c.1200G>A ENSP00000349297.5:p.Val400=
ENST00000542255.6:c.58G>A
ENST00000543245.6:c.1269G>A ENSP00000438689.2:p.Val423=
ENST00000578579.2:n.371G>A
ENST00000578711.1:n.157G>A
ENST00000578824.5:n.616G>A
ENST00000579425.5:n.224G>A
ENST00000579546.1:c.37G>A
ENST00000583858.5:c.229G>A
ENST00000585203.6:n.408G>A
NM_000018.3:c.1200G>A NP_000009.1:p.Val400=
NM_001033859.2:c.1134G>A NP_001029031.1:p.Val378=
NM_001270447.1:c.1269G>A NP_001257376.1:p.Val423=
NM_001270448.1:c.972G>A NP_001257377.1:p.Val324=
XM_006721516.2:c.1200G>A XP_006721579.2:p.Val400=
XM_011523829.1:c.1200G>A XP_011522131.1:p.Val400=
XM_011523830.1:c.1200G>A XP_011522132.1:p.Val400=
XR_934021.1:n.1307G>A
XR_934022.1:n.1307G>A
XR_934023.1:n.1307G>A
XM_006721516.3:c.1200G>A XP_006721579.2:p.Val400=
XM_011523829.2:c.1200G>A XP_011522131.1:p.Val400=
XM_011523830.2:c.1200G>A XP_011522132.1:p.Val400=
XM_024450741.1:c.1200G>A XP_024306509.1:p.Val400=
XR_934021.2:n.1259G>A
XR_934022.2:n.1259G>A
XR_934023.2:n.1259G>A
NM_000018.4:c.1200G>A MANE Select NP_000009.1:p.Val400=
NM_001033859.3:c.1134G>A NP_001029031.1:p.Val378=
NM_001270447.2:c.1269G>A NP_001257376.1:p.Val423=
NM_001270448.2:c.972G>A NP_001257377.1:p.Val324=
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