Canonical Allele Identifier: CA2245716388
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7225042C= , CM000679.2:g.7225042C= GRCh38
NC_000017.10:g.7128361C= , CM000679.1:g.7128361C= GRCh37
NC_000017.9:g.7069085C= NCBI36
NG_007975.1:g.10209C=
NG_008391.2:g.9G=
NG_033038.1:g.14503G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1913C= MANE Select ENSP00000349297.5:p.Ser638=
ENST00000322910.9:c.*1868C= ENSP00000325395.5:n.*1868C=
ENST00000350303.9:c.1847C= ENSP00000344152.5:p.Ser616=
ENST00000356839.9:c.1913C= ENSP00000349297.5:p.Ser638=
ENST00000542255.6:c.792C=
ENST00000543245.6:c.1982C= ENSP00000438689.2:p.Ser661=
ENST00000578033.1:n.338C=
ENST00000578319.5:n.494C=
ENST00000578711.1:n.1538C=
ENST00000578809.5:n.485C=
ENST00000579425.5:n.1029C=
ENST00000583848.5:c.279C= ENSP00000466487.1:n.279C=
ENST00000583850.5:n.684C=
ENST00000583858.5:c.844C=
NM_000018.3:c.1913C= NP_000009.1:p.Ser638=
NM_001033859.2:c.1847C= NP_001029031.1:p.Ser616=
NM_001270447.1:c.1982C= NP_001257376.1:p.Ser661=
NM_001270448.1:c.1685C= NP_001257377.1:p.Ser562=
XM_006721516.2:c.1934C= XP_006721579.2:p.Ser645=
XM_011523829.1:c.1832C= XP_011522131.1:p.Ser611=
XM_011523830.1:c.1811C= XP_011522132.1:p.Ser604=
XR_934021.1:n.2016C=
XR_934022.1:n.1922C=
XR_934023.1:n.1943C=
XM_006721516.3:c.1934C= XP_006721579.2:p.Ser645=
XM_011523829.2:c.1832C= XP_011522131.1:p.Ser611=
XM_011523830.2:c.1811C= XP_011522132.1:p.Ser604=
XM_024450741.1:c.1901C= XP_024306509.1:p.Ser634=
XR_934021.2:n.1968C=
XR_934022.2:n.1874C=
XR_934023.2:n.1895C=
NM_000018.4:c.1913C= MANE Select NP_000009.1:p.Ser638=
NM_001033859.3:c.1847C= NP_001029031.1:p.Ser616=
NM_001270447.2:c.1982C= NP_001257376.1:p.Ser661=
NM_001270448.2:c.1685C= NP_001257377.1:p.Ser562=