Canonical Allele Identifier: CA397725235
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224200A>T , CM000679.2:g.7224200A>T GRCh38
NC_000017.10:g.7127519A>T , CM000679.1:g.7127519A>T GRCh37
NC_000017.9:g.7068243A>T NCBI36
NG_007975.1:g.9367A>T
NG_008391.2:g.851T>A
NG_033038.1:g.15345T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1489A>T MANE Select ENSP00000349297.5:p.Asn497Tyr
ENST00000322910.9:c.*1444A>T ENSP00000325395.5:n.*1444A>T
ENST00000350303.9:c.1423A>T ENSP00000344152.5:p.Asn475Tyr
ENST00000356839.9:c.1489A>T ENSP00000349297.5:p.Asn497Tyr
ENST00000542255.6:c.347A>T
ENST00000543245.6:c.1558A>T ENSP00000438689.2:p.Asn520Tyr
ENST00000578711.1:n.696A>T
ENST00000579391.1:n.97A>T
ENST00000579425.5:n.605A>T
ENST00000579546.1:c.272-121A>T
ENST00000579894.5:n.276A>T
ENST00000583074.5:n.154-121A>T
ENST00000583850.5:n.264A>T
ENST00000583858.5:c.464-121A>T
ENST00000585203.6:n.680A>T
NM_000018.3:c.1489A>T NP_000009.1:p.Asn497Tyr
NM_001033859.2:c.1423A>T NP_001029031.1:p.Asn475Tyr
NM_001270447.1:c.1558A>T NP_001257376.1:p.Asn520Tyr
NM_001270448.1:c.1261A>T NP_001257377.1:p.Asn421Tyr
XM_006721516.2:c.1489A>T XP_006721579.2:p.Asn497Tyr
XM_011523829.1:c.1435-121A>T XP_011522131.1:n.1435-121A>T
XM_011523830.1:c.1435-121A>T XP_011522132.1:n.1435-121A>T
XR_934021.1:n.1596A>T
XR_934022.1:n.1542-121A>T
XR_934023.1:n.1542-121A>T
XM_006721516.3:c.1489A>T XP_006721579.2:p.Asn497Tyr
XM_011523829.2:c.1435-121A>T XP_011522131.1:n.1435-121A>T
XM_011523830.2:c.1435-121A>T XP_011522132.1:n.1435-121A>T
XM_024450741.1:c.1435-121A>T XP_024306509.1:n.1435-121A>T
XR_934021.2:n.1548A>T
XR_934022.2:n.1494-121A>T
XR_934023.2:n.1494-121A>T
NM_000018.4:c.1489A>T MANE Select NP_000009.1:p.Asn497Tyr
NM_001033859.3:c.1423A>T NP_001029031.1:p.Asn475Tyr
NM_001270447.2:c.1558A>T NP_001257376.1:p.Asn520Tyr
NM_001270448.2:c.1261A>T NP_001257377.1:p.Asn421Tyr