Canonical Allele Identifier: CA397724878
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223871T>A , CM000679.2:g.7223871T>A GRCh38
NC_000017.10:g.7127190T>A , CM000679.1:g.7127190T>A GRCh37
NC_000017.9:g.7067914T>A NCBI36
NG_007975.1:g.9038T>A
NG_008391.2:g.1180A>T
NG_033038.1:g.15674A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1328T>A MANE Select ENSP00000349297.5:p.Met443Lys
ENST00000322910.9:c.*1283T>A ENSP00000325395.5:n.*1283T>A
ENST00000350303.9:c.1262T>A ENSP00000344152.5:p.Met421Lys
ENST00000356839.9:c.1328T>A ENSP00000349297.5:p.Met443Lys
ENST00000542255.6:c.186T>A
ENST00000543245.6:c.1397T>A ENSP00000438689.2:p.Met466Lys
ENST00000578711.1:n.367T>A
ENST00000579425.5:n.352T>A
ENST00000579546.1:c.165T>A
ENST00000583074.5:n.47T>A
ENST00000583850.5:n.103T>A
ENST00000583858.5:c.357T>A
ENST00000585203.6:n.523+13T>A
NM_000018.3:c.1328T>A NP_000009.1:p.Met443Lys
NM_001033859.2:c.1262T>A NP_001029031.1:p.Met421Lys
NM_001270447.1:c.1397T>A NP_001257376.1:p.Met466Lys
NM_001270448.1:c.1100T>A NP_001257377.1:p.Met367Lys
XM_006721516.2:c.1328T>A XP_006721579.2:p.Met443Lys
XM_011523829.1:c.1328T>A XP_011522131.1:p.Met443Lys
XM_011523830.1:c.1328T>A XP_011522132.1:p.Met443Lys
XR_934021.1:n.1435T>A
XR_934022.1:n.1435T>A
XR_934023.1:n.1435T>A
XM_006721516.3:c.1328T>A XP_006721579.2:p.Met443Lys
XM_011523829.2:c.1328T>A XP_011522131.1:p.Met443Lys
XM_011523830.2:c.1328T>A XP_011522132.1:p.Met443Lys
XM_024450741.1:c.1328T>A XP_024306509.1:p.Met443Lys
XR_934021.2:n.1387T>A
XR_934022.2:n.1387T>A
XR_934023.2:n.1387T>A
NM_000018.4:c.1328T>A MANE Select NP_000009.1:p.Met443Lys
NM_001033859.3:c.1262T>A NP_001029031.1:p.Met421Lys
NM_001270447.2:c.1397T>A NP_001257376.1:p.Met466Lys
NM_001270448.2:c.1100T>A NP_001257377.1:p.Met367Lys