Canonical Allele Identifier: CA2245700650
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221851A= , CM000679.2:g.7221851A= GRCh38
NC_000017.10:g.7125170A= , CM000679.1:g.7125170A= GRCh37
NC_000017.9:g.7065894A= NCBI36
NG_007975.1:g.7018A=
NG_008391.2:g.3200T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.623-101A= MANE Select ENSP00000349297.5:n.623-101A=
ENST00000322910.9:c.*578-101A= ENSP00000325395.5:n.*578-101A=
ENST00000350303.9:c.557-101A= ENSP00000344152.5:n.557-101A=
ENST00000356839.9:c.623-101A= ENSP00000349297.5:n.623-101A=
ENST00000543245.6:c.692-101A= ENSP00000438689.2:n.692-101A=
ENST00000577191.5:n.700-101A=
ENST00000577857.5:n.439-101A=
ENST00000579286.5:n.804-101A=
ENST00000579886.2:c.461-101A= ENSP00000463246.1:n.461-101A=
ENST00000580365.1:n.354-101A=
ENST00000581378.5:c.341-101A=
ENST00000581562.5:n.525-101A=
ENST00000583312.5:c.623-86A= ENSP00000467920.1:n.623-86A=
ENST00000583760.1:n.405-101A=
NM_000018.3:c.623-101A= NP_000009.1:n.623-101A=
NM_001033859.2:c.557-101A= NP_001029031.1:n.557-101A=
NM_001270447.1:c.692-101A= NP_001257376.1:n.692-101A=
NM_001270448.1:c.395-101A= NP_001257377.1:n.395-101A=
XM_006721516.2:c.623-101A= XP_006721579.2:n.623-101A=
XM_011523829.1:c.623-101A= XP_011522131.1:n.623-101A=
XM_011523830.1:c.623-101A= XP_011522132.1:n.623-101A=
XR_934021.1:n.730-101A=
XR_934022.1:n.730-101A=
XR_934023.1:n.730-101A=
XM_006721516.3:c.623-101A= XP_006721579.2:n.623-101A=
XM_011523829.2:c.623-101A= XP_011522131.1:n.623-101A=
XM_011523830.2:c.623-101A= XP_011522132.1:n.623-101A=
XM_024450741.1:c.623-101A= XP_024306509.1:n.623-101A=
XR_934021.2:n.682-101A=
XR_934022.2:n.682-101A=
XR_934023.2:n.682-101A=
NM_000018.4:c.623-101A= MANE Select NP_000009.1:n.623-101A=
NM_001033859.3:c.557-101A= NP_001029031.1:n.557-101A=
NM_001270447.2:c.692-101A= NP_001257376.1:n.692-101A=
NM_001270448.2:c.395-101A= NP_001257377.1:n.395-101A=