Canonical Allele Identifier: CA2245701112
Gene: ACADVL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222105C= , CM000679.2:g.7222105C= GRCh38
NC_000017.10:g.7125424C= , CM000679.1:g.7125424C= GRCh37
NC_000017.9:g.7066148C= NCBI36
NG_007975.1:g.7272C=
NG_008391.2:g.2946G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.752+24C= MANE Select ENSP00000349297.5:n.752+24C=
ENST00000322910.9:c.*707+24C= ENSP00000325395.5:n.*707+24C=
ENST00000350303.9:c.686+24C= ENSP00000344152.5:n.686+24C=
ENST00000356839.9:c.752+24C= ENSP00000349297.5:n.752+24C=
ENST00000543245.6:c.821+24C= ENSP00000438689.2:n.821+24C=
ENST00000577191.5:n.853C=
ENST00000581378.5:c.470+24C=
ENST00000582379.1:n.136+24C=
ENST00000583760.1:n.558C=
NM_000018.3:c.752+24C= NP_000009.1:n.752+24C=
NM_001033859.2:c.686+24C= NP_001029031.1:n.686+24C=
NM_001270447.1:c.821+24C= NP_001257376.1:n.821+24C=
NM_001270448.1:c.524+24C= NP_001257377.1:n.524+24C=
XM_006721516.2:c.752+24C= XP_006721579.2:n.752+24C=
XM_011523829.1:c.752+24C= XP_011522131.1:n.752+24C=
XM_011523830.1:c.752+24C= XP_011522132.1:n.752+24C=
XR_934021.1:n.859+24C=
XR_934022.1:n.859+24C=
XR_934023.1:n.859+24C=
XM_006721516.3:c.752+24C= XP_006721579.2:n.752+24C=
XM_011523829.2:c.752+24C= XP_011522131.1:n.752+24C=
XM_011523830.2:c.752+24C= XP_011522132.1:n.752+24C=
XM_024450741.1:c.752+24C= XP_024306509.1:n.752+24C=
XR_934021.2:n.811+24C=
XR_934022.2:n.811+24C=
XR_934023.2:n.811+24C=
NM_000018.4:c.752+24C= MANE Select NP_000009.1:n.752+24C=
NM_001033859.3:c.686+24C= NP_001029031.1:n.686+24C=
NM_001270447.2:c.821+24C= NP_001257376.1:n.821+24C=
NM_001270448.2:c.524+24C= NP_001257377.1:n.524+24C=
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