Canonical Allele Identifier: CA397725232
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224198G>A , CM000679.2:g.7224198G>A GRCh38
NC_000017.10:g.7127517G>A , CM000679.1:g.7127517G>A GRCh37
NC_000017.9:g.7068241G>A NCBI36
NG_007975.1:g.9365G>A
NG_008391.2:g.853C>T
NG_033038.1:g.15347C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1487G>A MANE Select ENSP00000349297.5:p.Gly496Glu
ENST00000322910.9:c.*1442G>A ENSP00000325395.5:n.*1442G>A
ENST00000350303.9:c.1421G>A ENSP00000344152.5:p.Gly474Glu
ENST00000356839.9:c.1487G>A ENSP00000349297.5:p.Gly496Glu
ENST00000542255.6:c.345G>A
ENST00000543245.6:c.1556G>A ENSP00000438689.2:p.Gly519Glu
ENST00000578711.1:n.694G>A
ENST00000579391.1:n.95G>A
ENST00000579425.5:n.603G>A
ENST00000579546.1:c.272-123G>A
ENST00000579894.5:n.274G>A
ENST00000583074.5:n.154-123G>A
ENST00000583850.5:n.262G>A
ENST00000583858.5:c.464-123G>A
ENST00000585203.6:n.678G>A
NM_000018.3:c.1487G>A NP_000009.1:p.Gly496Glu
NM_001033859.2:c.1421G>A NP_001029031.1:p.Gly474Glu
NM_001270447.1:c.1556G>A NP_001257376.1:p.Gly519Glu
NM_001270448.1:c.1259G>A NP_001257377.1:p.Gly420Glu
XM_006721516.2:c.1487G>A XP_006721579.2:p.Gly496Glu
XM_011523829.1:c.1435-123G>A XP_011522131.1:n.1435-123G>A
XM_011523830.1:c.1435-123G>A XP_011522132.1:n.1435-123G>A
XR_934021.1:n.1594G>A
XR_934022.1:n.1542-123G>A
XR_934023.1:n.1542-123G>A
XM_006721516.3:c.1487G>A XP_006721579.2:p.Gly496Glu
XM_011523829.2:c.1435-123G>A XP_011522131.1:n.1435-123G>A
XM_011523830.2:c.1435-123G>A XP_011522132.1:n.1435-123G>A
XM_024450741.1:c.1435-123G>A XP_024306509.1:n.1435-123G>A
XR_934021.2:n.1546G>A
XR_934022.2:n.1494-123G>A
XR_934023.2:n.1494-123G>A
NM_000018.4:c.1487G>A MANE Select NP_000009.1:p.Gly496Glu
NM_001033859.3:c.1421G>A NP_001029031.1:p.Gly474Glu
NM_001270447.2:c.1556G>A NP_001257376.1:p.Gly519Glu
NM_001270448.2:c.1259G>A NP_001257377.1:p.Gly420Glu