Canonical Allele Identifier: CA2245700181
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221595G= , CM000679.2:g.7221595G= GRCh38
NC_000017.10:g.7124914G= , CM000679.1:g.7124914G= GRCh37
NC_000017.9:g.7065638G= NCBI36
NG_007975.1:g.6762G=
NG_008391.2:g.3456C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.535G= MANE Select ENSP00000349297.5:p.Gly179=
ENST00000322910.9:c.*490G= ENSP00000325395.5:n.*490G=
ENST00000350303.9:c.469G= ENSP00000344152.5:p.Gly157=
ENST00000356839.9:c.535G= ENSP00000349297.5:p.Gly179=
ENST00000543245.6:c.604G= ENSP00000438689.2:p.Gly202=
ENST00000577191.5:n.612G=
ENST00000577433.5:n.743G=
ENST00000577857.5:n.351G=
ENST00000579286.5:n.716G=
ENST00000579886.2:c.373G= ENSP00000463246.1:p.Gly125=
ENST00000580365.1:n.266G=
ENST00000581378.5:c.253G=
ENST00000581562.5:n.525-357G=
ENST00000582166.1:n.516G=
ENST00000583312.5:c.535G= ENSP00000467920.1:p.Gly179=
ENST00000583760.1:n.317G=
NM_000018.3:c.535G= NP_000009.1:p.Gly179=
NM_001033859.2:c.469G= NP_001029031.1:p.Gly157=
NM_001270447.1:c.604G= NP_001257376.1:p.Gly202=
NM_001270448.1:c.307G= NP_001257377.1:p.Gly103=
XM_006721516.2:c.535G= XP_006721579.2:p.Gly179=
XM_011523829.1:c.535G= XP_011522131.1:p.Gly179=
XM_011523830.1:c.535G= XP_011522132.1:p.Gly179=
XR_934021.1:n.642G=
XR_934022.1:n.642G=
XR_934023.1:n.642G=
XM_006721516.3:c.535G= XP_006721579.2:p.Gly179=
XM_011523829.2:c.535G= XP_011522131.1:p.Gly179=
XM_011523830.2:c.535G= XP_011522132.1:p.Gly179=
XM_024450741.1:c.535G= XP_024306509.1:p.Gly179=
XR_934021.2:n.594G=
XR_934022.2:n.594G=
XR_934023.2:n.594G=
NM_000018.4:c.535G= MANE Select NP_000009.1:p.Gly179=
NM_001033859.3:c.469G= NP_001029031.1:p.Gly157=
NM_001270447.2:c.604G= NP_001257376.1:p.Gly202=
NM_001270448.2:c.307G= NP_001257377.1:p.Gly103=