Canonical Allele Identifier: CA2245709330
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222704A= , CM000679.2:g.7222704A= GRCh38
NC_000017.10:g.7126023A= , CM000679.1:g.7126023A= GRCh37
NC_000017.9:g.7066747A= NCBI36
NG_007975.1:g.7871A=
NG_008391.2:g.2347T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.916A= MANE Select ENSP00000349297.5:p.Asn306=
ENST00000322910.9:c.*871A= ENSP00000325395.5:n.*871A=
ENST00000350303.9:c.850A= ENSP00000344152.5:p.Asn284=
ENST00000356839.9:c.916A= ENSP00000349297.5:p.Asn306=
ENST00000543245.6:c.985A= ENSP00000438689.2:p.Asn329=
ENST00000578824.5:n.65A=
ENST00000581378.5:c.634A=
ENST00000582379.1:n.300A=
NM_000018.3:c.916A= NP_000009.1:p.Asn306=
NM_001033859.2:c.850A= NP_001029031.1:p.Asn284=
NM_001270447.1:c.985A= NP_001257376.1:p.Asn329=
NM_001270448.1:c.688A= NP_001257377.1:p.Asn230=
XM_006721516.2:c.916A= XP_006721579.2:p.Asn306=
XM_011523829.1:c.916A= XP_011522131.1:p.Asn306=
XM_011523830.1:c.916A= XP_011522132.1:p.Asn306=
XR_934021.1:n.1023A=
XR_934022.1:n.1023A=
XR_934023.1:n.1023A=
XM_006721516.3:c.916A= XP_006721579.2:p.Asn306=
XM_011523829.2:c.916A= XP_011522131.1:p.Asn306=
XM_011523830.2:c.916A= XP_011522132.1:p.Asn306=
XM_024450741.1:c.916A= XP_024306509.1:p.Asn306=
XR_934021.2:n.975A=
XR_934022.2:n.975A=
XR_934023.2:n.975A=
NM_000018.4:c.916A= MANE Select NP_000009.1:p.Asn306=
NM_001033859.3:c.850A= NP_001029031.1:p.Asn284=
NM_001270447.2:c.985A= NP_001257376.1:p.Asn329=
NM_001270448.2:c.688A= NP_001257377.1:p.Asn230=