Canonical Allele Identifier: CA2245713360
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224208C= , CM000679.2:g.7224208C= GRCh38
NC_000017.10:g.7127527C= , CM000679.1:g.7127527C= GRCh37
NC_000017.9:g.7068251C= NCBI36
NG_007975.1:g.9375C=
NG_008391.2:g.843G=
NG_033038.1:g.15337G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1497C= MANE Select ENSP00000349297.5:p.Gly499=
ENST00000322910.9:c.*1452C= ENSP00000325395.5:n.*1452C=
ENST00000350303.9:c.1431C= ENSP00000344152.5:p.Gly477=
ENST00000356839.9:c.1497C= ENSP00000349297.5:p.Gly499=
ENST00000542255.6:c.355C=
ENST00000543245.6:c.1566C= ENSP00000438689.2:p.Gly522=
ENST00000578711.1:n.704C=
ENST00000579391.1:n.105C=
ENST00000579425.5:n.613C=
ENST00000579546.1:c.272-113C=
ENST00000579894.5:n.284C=
ENST00000583074.5:n.154-113C=
ENST00000583850.5:n.272C=
ENST00000583858.5:c.464-113C=
ENST00000585203.6:n.688C=
NM_000018.3:c.1497C= NP_000009.1:p.Gly499=
NM_001033859.2:c.1431C= NP_001029031.1:p.Gly477=
NM_001270447.1:c.1566C= NP_001257376.1:p.Gly522=
NM_001270448.1:c.1269C= NP_001257377.1:p.Gly423=
XM_006721516.2:c.1497C= XP_006721579.2:p.Gly499=
XM_011523829.1:c.1435-113C= XP_011522131.1:n.1435-113C=
XM_011523830.1:c.1435-113C= XP_011522132.1:n.1435-113C=
XR_934021.1:n.1604C=
XR_934022.1:n.1542-113C=
XR_934023.1:n.1542-113C=
XM_006721516.3:c.1497C= XP_006721579.2:p.Gly499=
XM_011523829.2:c.1435-113C= XP_011522131.1:n.1435-113C=
XM_011523830.2:c.1435-113C= XP_011522132.1:n.1435-113C=
XM_024450741.1:c.1435-113C= XP_024306509.1:n.1435-113C=
XR_934021.2:n.1556C=
XR_934022.2:n.1494-113C=
XR_934023.2:n.1494-113C=
NM_000018.4:c.1497C= MANE Select NP_000009.1:p.Gly499=
NM_001033859.3:c.1431C= NP_001029031.1:p.Gly477=
NM_001270447.2:c.1566C= NP_001257376.1:p.Gly522=
NM_001270448.2:c.1269C= NP_001257377.1:p.Gly423=