Canonical Allele Identifier: CA2245711675
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223715C= , CM000679.2:g.7223715C= GRCh38
NC_000017.10:g.7127034C= , CM000679.1:g.7127034C= GRCh37
NC_000017.9:g.7067758C= NCBI36
NG_007975.1:g.8882C=
NG_008391.2:g.1336G=
NG_033038.1:g.15830G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1254C= MANE Select ENSP00000349297.5:p.Ser418=
ENST00000322910.9:c.*1209C= ENSP00000325395.5:n.*1209C=
ENST00000350303.9:c.1188C= ENSP00000344152.5:p.Ser396=
ENST00000356839.9:c.1254C= ENSP00000349297.5:p.Ser418=
ENST00000542255.6:c.112C=
ENST00000543245.6:c.1323C= ENSP00000438689.2:p.Ser441=
ENST00000578579.2:n.425C=
ENST00000578711.1:n.211C=
ENST00000578824.5:n.670C=
ENST00000579425.5:n.278C=
ENST00000579546.1:c.91C=
ENST00000583850.5:n.29C=
ENST00000583858.5:c.283C=
ENST00000585203.6:n.462C=
NM_000018.3:c.1254C= NP_000009.1:p.Ser418=
NM_001033859.2:c.1188C= NP_001029031.1:p.Ser396=
NM_001270447.1:c.1323C= NP_001257376.1:p.Ser441=
NM_001270448.1:c.1026C= NP_001257377.1:p.Ser342=
XM_006721516.2:c.1254C= XP_006721579.2:p.Ser418=
XM_011523829.1:c.1254C= XP_011522131.1:p.Ser418=
XM_011523830.1:c.1254C= XP_011522132.1:p.Ser418=
XR_934021.1:n.1361C=
XR_934022.1:n.1361C=
XR_934023.1:n.1361C=
XM_006721516.3:c.1254C= XP_006721579.2:p.Ser418=
XM_011523829.2:c.1254C= XP_011522131.1:p.Ser418=
XM_011523830.2:c.1254C= XP_011522132.1:p.Ser418=
XM_024450741.1:c.1254C= XP_024306509.1:p.Ser418=
XR_934021.2:n.1313C=
XR_934022.2:n.1313C=
XR_934023.2:n.1313C=
NM_000018.4:c.1254C= MANE Select NP_000009.1:p.Ser418=
NM_001033859.3:c.1188C= NP_001029031.1:p.Ser396=
NM_001270447.2:c.1323C= NP_001257376.1:p.Ser441=
NM_001270448.2:c.1026C= NP_001257377.1:p.Ser342=