Canonical Allele Identifier: CA397725087
Gene: ACADVL HGNC NCBI

Linked Data

ClinVar Variation Id: 958459
ClinVar RCV Id: RCV001231630
dbSNP Id: rs2071357482
MyVariant Identifiers: chr17:g.7127381G>A (hg19) chr17:g.7224062G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224062G>A , CM000679.2:g.7224062G>A GRCh38
NC_000017.10:g.7127381G>A , CM000679.1:g.7127381G>A GRCh37
NC_000017.9:g.7068105G>A NCBI36
NG_007975.1:g.9229G>A
NG_008391.2:g.989C>T
NG_033038.1:g.15483C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1427G>A MANE Select ENSP00000349297.5:p.Gly476Asp
ENST00000322910.9:c.*1382G>A ENSP00000325395.5:n.*1382G>A
ENST00000350303.9:c.1361G>A ENSP00000344152.5:p.Gly454Asp
ENST00000356839.9:c.1427G>A ENSP00000349297.5:p.Gly476Asp
ENST00000542255.6:c.285G>A
ENST00000543245.6:c.1496G>A ENSP00000438689.2:p.Gly499Asp
ENST00000578711.1:n.558G>A
ENST00000579425.5:n.543G>A
ENST00000579546.1:c.264G>A
ENST00000579894.5:n.138G>A
ENST00000583074.5:n.146G>A
ENST00000583850.5:n.202G>A
ENST00000583858.5:c.456G>A
ENST00000585203.6:n.618G>A
NM_000018.3:c.1427G>A NP_000009.1:p.Gly476Asp
NM_001033859.2:c.1361G>A NP_001029031.1:p.Gly454Asp
NM_001270447.1:c.1496G>A NP_001257376.1:p.Gly499Asp
NM_001270448.1:c.1199G>A NP_001257377.1:p.Gly400Asp
XM_006721516.2:c.1427G>A XP_006721579.2:p.Gly476Asp
XM_011523829.1:c.1427G>A XP_011522131.1:p.Gly476Asp
XM_011523830.1:c.1427G>A XP_011522132.1:p.Gly476Asp
XR_934021.1:n.1534G>A
XR_934022.1:n.1534G>A
XR_934023.1:n.1534G>A
XM_006721516.3:c.1427G>A XP_006721579.2:p.Gly476Asp
XM_011523829.2:c.1427G>A XP_011522131.1:p.Gly476Asp
XM_011523830.2:c.1427G>A XP_011522132.1:p.Gly476Asp
XM_024450741.1:c.1427G>A XP_024306509.1:p.Gly476Asp
XR_934021.2:n.1486G>A
XR_934022.2:n.1486G>A
XR_934023.2:n.1486G>A
NM_000018.4:c.1427G>A MANE Select NP_000009.1:p.Gly476Asp
NM_001033859.3:c.1361G>A NP_001029031.1:p.Gly454Asp
NM_001270447.2:c.1496G>A NP_001257376.1:p.Gly499Asp
NM_001270448.2:c.1199G>A NP_001257377.1:p.Gly400Asp
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