Canonical Allele Identifier: CA2245709933
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222848G= , CM000679.2:g.7222848G= GRCh38
NC_000017.10:g.7126167G= , CM000679.1:g.7126167G= GRCh37
NC_000017.9:g.7066891G= NCBI36
NG_007975.1:g.8015G=
NG_008391.2:g.2203C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1060G= MANE Select ENSP00000349297.5:p.Gly354=
ENST00000322910.9:c.*1015G= ENSP00000325395.5:n.*1015G=
ENST00000350303.9:c.994G= ENSP00000344152.5:p.Gly332=
ENST00000356839.9:c.1060G= ENSP00000349297.5:p.Gly354=
ENST00000543245.6:c.1129G= ENSP00000438689.2:p.Gly377=
ENST00000578824.5:n.209G=
ENST00000582379.1:n.444G=
ENST00000583858.5:c.89G=
ENST00000585203.6:n.1G=
NM_000018.3:c.1060G= NP_000009.1:p.Gly354=
NM_001033859.2:c.994G= NP_001029031.1:p.Gly332=
NM_001270447.1:c.1129G= NP_001257376.1:p.Gly377=
NM_001270448.1:c.832G= NP_001257377.1:p.Gly278=
XM_006721516.2:c.1060G= XP_006721579.2:p.Gly354=
XM_011523829.1:c.1060G= XP_011522131.1:p.Gly354=
XM_011523830.1:c.1060G= XP_011522132.1:p.Gly354=
XR_934021.1:n.1167G=
XR_934022.1:n.1167G=
XR_934023.1:n.1167G=
XM_006721516.3:c.1060G= XP_006721579.2:p.Gly354=
XM_011523829.2:c.1060G= XP_011522131.1:p.Gly354=
XM_011523830.2:c.1060G= XP_011522132.1:p.Gly354=
XM_024450741.1:c.1060G= XP_024306509.1:p.Gly354=
XR_934021.2:n.1119G=
XR_934022.2:n.1119G=
XR_934023.2:n.1119G=
NM_000018.4:c.1060G= MANE Select NP_000009.1:p.Gly354=
NM_001033859.3:c.994G= NP_001029031.1:p.Gly332=
NM_001270447.2:c.1129G= NP_001257376.1:p.Gly377=
NM_001270448.2:c.832G= NP_001257377.1:p.Gly278=