Canonical Allele Identifier: CA397724062
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222753T>A , CM000679.2:g.7222753T>A GRCh38
NC_000017.10:g.7126072T>A , CM000679.1:g.7126072T>A GRCh37
NC_000017.9:g.7066796T>A NCBI36
NG_007975.1:g.7920T>A
NG_008391.2:g.2298A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.965T>A MANE Select ENSP00000349297.5:p.Val322Glu
ENST00000322910.9:c.*920T>A ENSP00000325395.5:n.*920T>A
ENST00000350303.9:c.899T>A ENSP00000344152.5:p.Val300Glu
ENST00000356839.9:c.965T>A ENSP00000349297.5:p.Val322Glu
ENST00000543245.6:c.1034T>A ENSP00000438689.2:p.Val345Glu
ENST00000578824.5:n.114T>A
ENST00000581378.5:c.683T>A
ENST00000582379.1:n.349T>A
NM_000018.3:c.965T>A NP_000009.1:p.Val322Glu
NM_001033859.2:c.899T>A NP_001029031.1:p.Val300Glu
NM_001270447.1:c.1034T>A NP_001257376.1:p.Val345Glu
NM_001270448.1:c.737T>A NP_001257377.1:p.Val246Glu
XM_006721516.2:c.965T>A XP_006721579.2:p.Val322Glu
XM_011523829.1:c.965T>A XP_011522131.1:p.Val322Glu
XM_011523830.1:c.965T>A XP_011522132.1:p.Val322Glu
XR_934021.1:n.1072T>A
XR_934022.1:n.1072T>A
XR_934023.1:n.1072T>A
XM_006721516.3:c.965T>A XP_006721579.2:p.Val322Glu
XM_011523829.2:c.965T>A XP_011522131.1:p.Val322Glu
XM_011523830.2:c.965T>A XP_011522132.1:p.Val322Glu
XM_024450741.1:c.965T>A XP_024306509.1:p.Val322Glu
XR_934021.2:n.1024T>A
XR_934022.2:n.1024T>A
XR_934023.2:n.1024T>A
NM_000018.4:c.965T>A MANE Select NP_000009.1:p.Val322Glu
NM_001033859.3:c.899T>A NP_001029031.1:p.Val300Glu
NM_001270447.2:c.1034T>A NP_001257376.1:p.Val345Glu
NM_001270448.2:c.737T>A NP_001257377.1:p.Val246Glu