Canonical Allele Identifier: CA397725293
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224231A>C , CM000679.2:g.7224231A>C GRCh38
NC_000017.10:g.7127550A>C , CM000679.1:g.7127550A>C GRCh37
NC_000017.9:g.7068274A>C NCBI36
NG_007975.1:g.9398A>C
NG_008391.2:g.820T>G
NG_033038.1:g.15314T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1520A>C MANE Select ENSP00000349297.5:p.Lys507Thr
ENST00000322910.9:c.*1475A>C ENSP00000325395.5:n.*1475A>C
ENST00000350303.9:c.1454A>C ENSP00000344152.5:p.Lys485Thr
ENST00000356839.9:c.1520A>C ENSP00000349297.5:p.Lys507Thr
ENST00000542255.6:c.378A>C
ENST00000543245.6:c.1589A>C ENSP00000438689.2:p.Lys530Thr
ENST00000578319.5:n.15A>C
ENST00000578711.1:n.727A>C
ENST00000578809.5:n.15A>C
ENST00000579391.1:n.128A>C
ENST00000579425.5:n.636A>C
ENST00000579546.1:c.272-90A>C
ENST00000579894.5:n.307A>C
ENST00000583074.5:n.154-90A>C
ENST00000583850.5:n.295A>C
ENST00000583858.5:c.464-90A>C
ENST00000585203.6:n.711A>C
NM_000018.3:c.1520A>C NP_000009.1:p.Lys507Thr
NM_001033859.2:c.1454A>C NP_001029031.1:p.Lys485Thr
NM_001270447.1:c.1589A>C NP_001257376.1:p.Lys530Thr
NM_001270448.1:c.1292A>C NP_001257377.1:p.Lys431Thr
XM_006721516.2:c.1520A>C XP_006721579.2:p.Lys507Thr
XM_011523829.1:c.1435-90A>C XP_011522131.1:n.1435-90A>C
XM_011523830.1:c.1435-90A>C XP_011522132.1:n.1435-90A>C
XR_934021.1:n.1627A>C
XR_934022.1:n.1542-90A>C
XR_934023.1:n.1542-90A>C
XM_006721516.3:c.1520A>C XP_006721579.2:p.Lys507Thr
XM_011523829.2:c.1435-90A>C XP_011522131.1:n.1435-90A>C
XM_011523830.2:c.1435-90A>C XP_011522132.1:n.1435-90A>C
XM_024450741.1:c.1435-90A>C XP_024306509.1:n.1435-90A>C
XR_934021.2:n.1579A>C
XR_934022.2:n.1494-90A>C
XR_934023.2:n.1494-90A>C
NM_000018.4:c.1520A>C MANE Select NP_000009.1:p.Lys507Thr
NM_001033859.3:c.1454A>C NP_001029031.1:p.Lys485Thr
NM_001270447.2:c.1589A>C NP_001257376.1:p.Lys530Thr
NM_001270448.2:c.1292A>C NP_001257377.1:p.Lys431Thr