Canonical Allele Identifier: CA397725237
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1489A>C MANE Select ENSP00000349297.5:p.Asn497His
ENST00000322910.9:c.*1444A>C ENSP00000325395.5:n.*1444A>C
ENST00000350303.9:c.1423A>C ENSP00000344152.5:p.Asn475His
ENST00000356839.9:c.1489A>C ENSP00000349297.5:p.Asn497His
ENST00000542255.6:c.347A>C
ENST00000543245.6:c.1558A>C ENSP00000438689.2:p.Asn520His
ENST00000578711.1:n.696A>C
ENST00000579391.1:n.97A>C
ENST00000579425.5:n.605A>C
ENST00000579546.1:c.272-121A>C
ENST00000579894.5:n.276A>C
ENST00000583074.5:n.154-121A>C
ENST00000583850.5:n.264A>C
ENST00000583858.5:c.464-121A>C
ENST00000585203.6:n.680A>C
NM_000018.3:c.1489A>C NP_000009.1:p.Asn497His
NM_001033859.2:c.1423A>C NP_001029031.1:p.Asn475His
NM_001270447.1:c.1558A>C NP_001257376.1:p.Asn520His
NM_001270448.1:c.1261A>C NP_001257377.1:p.Asn421His
XM_006721516.2:c.1489A>C XP_006721579.2:p.Asn497His
XM_011523829.1:c.1435-121A>C XP_011522131.1:n.1435-121A>C
XM_011523830.1:c.1435-121A>C XP_011522132.1:n.1435-121A>C
XR_934021.1:n.1596A>C
XR_934022.1:n.1542-121A>C
XR_934023.1:n.1542-121A>C
XM_006721516.3:c.1489A>C XP_006721579.2:p.Asn497His
XM_011523829.2:c.1435-121A>C XP_011522131.1:n.1435-121A>C
XM_011523830.2:c.1435-121A>C XP_011522132.1:n.1435-121A>C
XM_024450741.1:c.1435-121A>C XP_024306509.1:n.1435-121A>C
XR_934021.2:n.1548A>C
XR_934022.2:n.1494-121A>C
XR_934023.2:n.1494-121A>C
NM_000018.4:c.1489A>C MANE Select NP_000009.1:p.Asn497His
NM_001033859.3:c.1423A>C NP_001029031.1:p.Asn475His
NM_001270447.2:c.1558A>C NP_001257376.1:p.Asn520His
NM_001270448.2:c.1261A>C NP_001257377.1:p.Asn421His