Canonical Allele Identifier: CA2245709524
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222752G= , CM000679.2:g.7222752G= GRCh38
NC_000017.10:g.7126071G= , CM000679.1:g.7126071G= GRCh37
NC_000017.9:g.7066795G= NCBI36
NG_007975.1:g.7919G=
NG_008391.2:g.2299C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.964G= MANE Select ENSP00000349297.5:p.Val322=
ENST00000322910.9:c.*919G= ENSP00000325395.5:n.*919G=
ENST00000350303.9:c.898G= ENSP00000344152.5:p.Val300=
ENST00000356839.9:c.964G= ENSP00000349297.5:p.Val322=
ENST00000543245.6:c.1033G= ENSP00000438689.2:p.Val345=
ENST00000578824.5:n.113G=
ENST00000581378.5:c.682G=
ENST00000582379.1:n.348G=
NM_000018.3:c.964G= NP_000009.1:p.Val322=
NM_001033859.2:c.898G= NP_001029031.1:p.Val300=
NM_001270447.1:c.1033G= NP_001257376.1:p.Val345=
NM_001270448.1:c.736G= NP_001257377.1:p.Val246=
XM_006721516.2:c.964G= XP_006721579.2:p.Val322=
XM_011523829.1:c.964G= XP_011522131.1:p.Val322=
XM_011523830.1:c.964G= XP_011522132.1:p.Val322=
XR_934021.1:n.1071G=
XR_934022.1:n.1071G=
XR_934023.1:n.1071G=
XM_006721516.3:c.964G= XP_006721579.2:p.Val322=
XM_011523829.2:c.964G= XP_011522131.1:p.Val322=
XM_011523830.2:c.964G= XP_011522132.1:p.Val322=
XM_024450741.1:c.964G= XP_024306509.1:p.Val322=
XR_934021.2:n.1023G=
XR_934022.2:n.1023G=
XR_934023.2:n.1023G=
NM_000018.4:c.964G= MANE Select NP_000009.1:p.Val322=
NM_001033859.3:c.898G= NP_001029031.1:p.Val300=
NM_001270447.2:c.1033G= NP_001257376.1:p.Val345=
NM_001270448.2:c.736G= NP_001257377.1:p.Val246=