Canonical Allele Identifier: CA2245700256
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221612C= , CM000679.2:g.7221612C= GRCh38
NC_000017.10:g.7124931C= , CM000679.1:g.7124931C= GRCh37
NC_000017.9:g.7065655C= NCBI36
NG_007975.1:g.6779C=
NG_008391.2:g.3439G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.552C= MANE Select ENSP00000349297.5:p.Ile184=
ENST00000322910.9:c.*507C= ENSP00000325395.5:n.*507C=
ENST00000350303.9:c.486C= ENSP00000344152.5:p.Ile162=
ENST00000356839.9:c.552C= ENSP00000349297.5:p.Ile184=
ENST00000543245.6:c.621C= ENSP00000438689.2:p.Ile207=
ENST00000577191.5:n.629C=
ENST00000577433.5:n.760C=
ENST00000577857.5:n.368C=
ENST00000579286.5:n.733C=
ENST00000579886.2:c.390C= ENSP00000463246.1:p.Ile130=
ENST00000580365.1:n.283C=
ENST00000581378.5:c.270C=
ENST00000581562.5:n.525-340C=
ENST00000582166.1:n.533C=
ENST00000583312.5:c.552C= ENSP00000467920.1:p.Ile184=
ENST00000583760.1:n.334C=
NM_000018.3:c.552C= NP_000009.1:p.Ile184=
NM_001033859.2:c.486C= NP_001029031.1:p.Ile162=
NM_001270447.1:c.621C= NP_001257376.1:p.Ile207=
NM_001270448.1:c.324C= NP_001257377.1:p.Ile108=
XM_006721516.2:c.552C= XP_006721579.2:p.Ile184=
XM_011523829.1:c.552C= XP_011522131.1:p.Ile184=
XM_011523830.1:c.552C= XP_011522132.1:p.Ile184=
XR_934021.1:n.659C=
XR_934022.1:n.659C=
XR_934023.1:n.659C=
XM_006721516.3:c.552C= XP_006721579.2:p.Ile184=
XM_011523829.2:c.552C= XP_011522131.1:p.Ile184=
XM_011523830.2:c.552C= XP_011522132.1:p.Ile184=
XM_024450741.1:c.552C= XP_024306509.1:p.Ile184=
XR_934021.2:n.611C=
XR_934022.2:n.611C=
XR_934023.2:n.611C=
NM_000018.4:c.552C= MANE Select NP_000009.1:p.Ile184=
NM_001033859.3:c.486C= NP_001029031.1:p.Ile162=
NM_001270447.2:c.621C= NP_001257376.1:p.Ile207=
NM_001270448.2:c.324C= NP_001257377.1:p.Ile108=