Canonical Allele Identifier: CA2245700773
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221952G= , CM000679.2:g.7221952G= GRCh38
NC_000017.10:g.7125271G= , CM000679.1:g.7125271G= GRCh37
NC_000017.9:g.7065995G= NCBI36
NG_007975.1:g.7119G=
NG_008391.2:g.3099C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.623G= MANE Select ENSP00000349297.5:p.Gly208=
ENST00000322910.9:c.*578G= ENSP00000325395.5:n.*578G=
ENST00000350303.9:c.557G= ENSP00000344152.5:p.Gly186=
ENST00000356839.9:c.623G= ENSP00000349297.5:p.Gly208=
ENST00000543245.6:c.692G= ENSP00000438689.2:p.Gly231=
ENST00000577191.5:n.700G=
ENST00000577857.5:n.439G=
ENST00000579286.5:n.804G=
ENST00000579886.2:c.461G= ENSP00000463246.1:p.Gly154=
ENST00000580365.1:n.354G=
ENST00000581378.5:c.341G=
ENST00000581562.5:n.525G=
ENST00000582379.1:n.7G=
ENST00000583312.5:c.638G= ENSP00000467920.1:p.Gly213=
ENST00000583760.1:n.405G=
NM_000018.3:c.623G= NP_000009.1:p.Gly208=
NM_001033859.2:c.557G= NP_001029031.1:p.Gly186=
NM_001270447.1:c.692G= NP_001257376.1:p.Gly231=
NM_001270448.1:c.395G= NP_001257377.1:p.Gly132=
XM_006721516.2:c.623G= XP_006721579.2:p.Gly208=
XM_011523829.1:c.623G= XP_011522131.1:p.Gly208=
XM_011523830.1:c.623G= XP_011522132.1:p.Gly208=
XR_934021.1:n.730G=
XR_934022.1:n.730G=
XR_934023.1:n.730G=
XM_006721516.3:c.623G= XP_006721579.2:p.Gly208=
XM_011523829.2:c.623G= XP_011522131.1:p.Gly208=
XM_011523830.2:c.623G= XP_011522132.1:p.Gly208=
XM_024450741.1:c.623G= XP_024306509.1:p.Gly208=
XR_934021.2:n.682G=
XR_934022.2:n.682G=
XR_934023.2:n.682G=
NM_000018.4:c.623G= MANE Select NP_000009.1:p.Gly208=
NM_001033859.3:c.557G= NP_001029031.1:p.Gly186=
NM_001270447.2:c.692G= NP_001257376.1:p.Gly231=
NM_001270448.2:c.395G= NP_001257377.1:p.Gly132=