Canonical Allele Identifier: CA397725287
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224228G>C , CM000679.2:g.7224228G>C GRCh38
NC_000017.10:g.7127547G>C , CM000679.1:g.7127547G>C GRCh37
NC_000017.9:g.7068271G>C NCBI36
NG_007975.1:g.9395G>C
NG_008391.2:g.823C>G
NG_033038.1:g.15317C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1517G>C MANE Select ENSP00000349297.5:p.Gly506Ala
ENST00000322910.9:c.*1472G>C ENSP00000325395.5:n.*1472G>C
ENST00000350303.9:c.1451G>C ENSP00000344152.5:p.Gly484Ala
ENST00000356839.9:c.1517G>C ENSP00000349297.5:p.Gly506Ala
ENST00000542255.6:c.375G>C
ENST00000543245.6:c.1586G>C ENSP00000438689.2:p.Gly529Ala
ENST00000578319.5:n.12G>C
ENST00000578711.1:n.724G>C
ENST00000578809.5:n.12G>C
ENST00000579391.1:n.125G>C
ENST00000579425.5:n.633G>C
ENST00000579546.1:c.272-93G>C
ENST00000579894.5:n.304G>C
ENST00000583074.5:n.154-93G>C
ENST00000583850.5:n.292G>C
ENST00000583858.5:c.464-93G>C
ENST00000585203.6:n.708G>C
NM_000018.3:c.1517G>C NP_000009.1:p.Gly506Ala
NM_001033859.2:c.1451G>C NP_001029031.1:p.Gly484Ala
NM_001270447.1:c.1586G>C NP_001257376.1:p.Gly529Ala
NM_001270448.1:c.1289G>C NP_001257377.1:p.Gly430Ala
XM_006721516.2:c.1517G>C XP_006721579.2:p.Gly506Ala
XM_011523829.1:c.1435-93G>C XP_011522131.1:n.1435-93G>C
XM_011523830.1:c.1435-93G>C XP_011522132.1:n.1435-93G>C
XR_934021.1:n.1624G>C
XR_934022.1:n.1542-93G>C
XR_934023.1:n.1542-93G>C
XM_006721516.3:c.1517G>C XP_006721579.2:p.Gly506Ala
XM_011523829.2:c.1435-93G>C XP_011522131.1:n.1435-93G>C
XM_011523830.2:c.1435-93G>C XP_011522132.1:n.1435-93G>C
XM_024450741.1:c.1435-93G>C XP_024306509.1:n.1435-93G>C
XR_934021.2:n.1576G>C
XR_934022.2:n.1494-93G>C
XR_934023.2:n.1494-93G>C
NM_000018.4:c.1517G>C MANE Select NP_000009.1:p.Gly506Ala
NM_001033859.3:c.1451G>C NP_001029031.1:p.Gly484Ala
NM_001270447.2:c.1586G>C NP_001257376.1:p.Gly529Ala
NM_001270448.2:c.1289G>C NP_001257377.1:p.Gly430Ala