Canonical Allele Identifier: CA2245700290
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221622G= , CM000679.2:g.7221622G= GRCh38
NC_000017.10:g.7124941G= , CM000679.1:g.7124941G= GRCh37
NC_000017.9:g.7065665G= NCBI36
NG_007975.1:g.6789G=
NG_008391.2:g.3429C=

Transcript Alleles

HGVS Amino-acid change
ENST00000356839.10:c.562G= MANE Select ENSP00000349297.5:p.Gly188=
ENST00000322910.9:c.*517G= ENSP00000325395.5:p.=
ENST00000350303.9:c.496G= ENSP00000344152.5:p.Gly166=
ENST00000356839.9:c.562G= ENSP00000349297.5:p.Gly188=
ENST00000543245.6:c.631G= ENSP00000438689.2:p.Gly211=
ENST00000577191.5:n.639G=
ENST00000577433.5:n.770G=
ENST00000577857.5:n.378G=
ENST00000579286.5:n.743G=
ENST00000579886.2:c.400G= ENSP00000463246.1:p.Gly134=
ENST00000580365.1:n.293G=
ENST00000581378.5:n.280G=
ENST00000581562.5:n.525-330G=
ENST00000582166.1:n.543G=
ENST00000583312.5:c.562G= ENSP00000467920.1:p.Gly188=
ENST00000583760.1:n.344G=
NM_000018.3:c.562G= NP_000009.1:p.Gly188=
NM_001033859.2:c.496G= NP_001029031.1:p.Gly166=
NM_001270447.1:c.631G= NP_001257376.1:p.Gly211=
NM_001270448.1:c.334G= NP_001257377.1:p.Gly112=
XM_006721516.2:c.562G= XP_006721579.2:p.Gly188=
XM_011523829.1:c.562G= XP_011522131.1:p.Gly188=
XM_011523830.1:c.562G= XP_011522132.1:p.Gly188=
XR_934021.1:n.669G=
XR_934022.1:n.669G=
XR_934023.1:n.669G=
XM_006721516.3:c.562G= XP_006721579.2:p.Gly188=
XM_011523829.2:c.562G= XP_011522131.1:p.Gly188=
XM_011523830.2:c.562G= XP_011522132.1:p.Gly188=
XM_024450741.1:c.562G= XP_024306509.1:p.Gly188=
XR_934021.2:n.621G=
XR_934022.2:n.621G=
XR_934023.2:n.621G=
NM_000018.4:c.562G= MANE Select NP_000009.1:p.Gly188=
NM_001033859.3:c.496G= NP_001029031.1:p.Gly166=
NM_001270447.2:c.631G= NP_001257376.1:p.Gly211=
NM_001270448.2:c.334G= NP_001257377.1:p.Gly112=