Canonical Allele Identifier: CA2245713343
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224207G= , CM000679.2:g.7224207G= GRCh38
NC_000017.10:g.7127526G= , CM000679.1:g.7127526G= GRCh37
NC_000017.9:g.7068250G= NCBI36
NG_007975.1:g.9374G=
NG_008391.2:g.844C=
NG_033038.1:g.15338C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1496G= MANE Select ENSP00000349297.5:p.Gly499=
ENST00000322910.9:c.*1451G= ENSP00000325395.5:n.*1451G=
ENST00000350303.9:c.1430G= ENSP00000344152.5:p.Gly477=
ENST00000356839.9:c.1496G= ENSP00000349297.5:p.Gly499=
ENST00000542255.6:c.354G=
ENST00000543245.6:c.1565G= ENSP00000438689.2:p.Gly522=
ENST00000578711.1:n.703G=
ENST00000579391.1:n.104G=
ENST00000579425.5:n.612G=
ENST00000579546.1:c.272-114G=
ENST00000579894.5:n.283G=
ENST00000583074.5:n.154-114G=
ENST00000583850.5:n.271G=
ENST00000583858.5:c.464-114G=
ENST00000585203.6:n.687G=
NM_000018.3:c.1496G= NP_000009.1:p.Gly499=
NM_001033859.2:c.1430G= NP_001029031.1:p.Gly477=
NM_001270447.1:c.1565G= NP_001257376.1:p.Gly522=
NM_001270448.1:c.1268G= NP_001257377.1:p.Gly423=
XM_006721516.2:c.1496G= XP_006721579.2:p.Gly499=
XM_011523829.1:c.1435-114G= XP_011522131.1:n.1435-114G=
XM_011523830.1:c.1435-114G= XP_011522132.1:n.1435-114G=
XR_934021.1:n.1603G=
XR_934022.1:n.1542-114G=
XR_934023.1:n.1542-114G=
XM_006721516.3:c.1496G= XP_006721579.2:p.Gly499=
XM_011523829.2:c.1435-114G= XP_011522131.1:n.1435-114G=
XM_011523830.2:c.1435-114G= XP_011522132.1:n.1435-114G=
XM_024450741.1:c.1435-114G= XP_024306509.1:n.1435-114G=
XR_934021.2:n.1555G=
XR_934022.2:n.1494-114G=
XR_934023.2:n.1494-114G=
NM_000018.4:c.1496G= MANE Select NP_000009.1:p.Gly499=
NM_001033859.3:c.1430G= NP_001029031.1:p.Gly477=
NM_001270447.2:c.1565G= NP_001257376.1:p.Gly522=
NM_001270448.2:c.1268G= NP_001257377.1:p.Gly423=