Canonical Allele Identifier: CA397723507
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222038T>A , CM000679.2:g.7222038T>A GRCh38
NC_000017.10:g.7125357T>A , CM000679.1:g.7125357T>A GRCh37
NC_000017.9:g.7066081T>A NCBI36
NG_007975.1:g.7205T>A
NG_008391.2:g.3013A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.709T>A MANE Select ENSP00000349297.5:p.Cys237Ser
ENST00000322910.9:c.*664T>A ENSP00000325395.5:n.*664T>A
ENST00000350303.9:c.643T>A ENSP00000344152.5:p.Cys215Ser
ENST00000356839.9:c.709T>A ENSP00000349297.5:p.Cys237Ser
ENST00000543245.6:c.778T>A ENSP00000438689.2:p.Cys260Ser
ENST00000577191.5:n.786T>A
ENST00000577857.5:n.525T>A
ENST00000579286.5:n.890T>A
ENST00000580365.1:n.440T>A
ENST00000581378.5:c.427T>A
ENST00000582379.1:n.93T>A
ENST00000583760.1:n.491T>A
NM_000018.3:c.709T>A NP_000009.1:p.Cys237Ser
NM_001033859.2:c.643T>A NP_001029031.1:p.Cys215Ser
NM_001270447.1:c.778T>A NP_001257376.1:p.Cys260Ser
NM_001270448.1:c.481T>A NP_001257377.1:p.Cys161Ser
XM_006721516.2:c.709T>A XP_006721579.2:p.Cys237Ser
XM_011523829.1:c.709T>A XP_011522131.1:p.Cys237Ser
XM_011523830.1:c.709T>A XP_011522132.1:p.Cys237Ser
XR_934021.1:n.816T>A
XR_934022.1:n.816T>A
XR_934023.1:n.816T>A
XM_006721516.3:c.709T>A XP_006721579.2:p.Cys237Ser
XM_011523829.2:c.709T>A XP_011522131.1:p.Cys237Ser
XM_011523830.2:c.709T>A XP_011522132.1:p.Cys237Ser
XM_024450741.1:c.709T>A XP_024306509.1:p.Cys237Ser
XR_934021.2:n.768T>A
XR_934022.2:n.768T>A
XR_934023.2:n.768T>A
NM_000018.4:c.709T>A MANE Select NP_000009.1:p.Cys237Ser
NM_001033859.3:c.643T>A NP_001029031.1:p.Cys215Ser
NM_001270447.2:c.778T>A NP_001257376.1:p.Cys260Ser
NM_001270448.2:c.481T>A NP_001257377.1:p.Cys161Ser