Canonical Allele Identifier: CA2245716461
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7225063G= , CM000679.2:g.7225063G= GRCh38
NC_000017.10:g.7128382G= , CM000679.1:g.7128382G= GRCh37
NC_000017.9:g.7069106G= NCBI36
NG_007975.1:g.10230G=
NG_033038.1:g.14482C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1934G= MANE Select ENSP00000349297.5:p.Gly645=
ENST00000322910.9:c.*1889G= ENSP00000325395.5:n.*1889G=
ENST00000350303.9:c.1868G= ENSP00000344152.5:p.Gly623=
ENST00000356839.9:c.1934G= ENSP00000349297.5:p.Gly645=
ENST00000542255.6:c.813G=
ENST00000543245.6:c.2003G= ENSP00000438689.2:p.Gly668=
ENST00000578033.1:n.359G=
ENST00000578319.5:n.515G=
ENST00000578711.1:n.1559G=
ENST00000578809.5:n.506G=
ENST00000579425.5:n.1050G=
ENST00000583848.5:c.300G= ENSP00000466487.1:n.300G=
ENST00000583850.5:n.705G=
ENST00000583858.5:c.865G=
NM_000018.3:c.1934G= NP_000009.1:p.Gly645=
NM_001033859.2:c.1868G= NP_001029031.1:p.Gly623=
NM_001270447.1:c.2003G= NP_001257376.1:p.Gly668=
NM_001270448.1:c.1706G= NP_001257377.1:p.Gly569=
XM_006721516.2:c.1955G= XP_006721579.2:p.Gly652=
XM_011523829.1:c.1853G= XP_011522131.1:p.Gly618=
XM_011523830.1:c.1832G= XP_011522132.1:p.Gly611=
XR_934021.1:n.2037G=
XR_934022.1:n.1943G=
XR_934023.1:n.1964G=
XM_006721516.3:c.1955G= XP_006721579.2:p.Gly652=
XM_011523829.2:c.1853G= XP_011522131.1:p.Gly618=
XM_011523830.2:c.1832G= XP_011522132.1:p.Gly611=
XM_024450741.1:c.1922G= XP_024306509.1:p.Gly641=
XR_934021.2:n.1989G=
XR_934022.2:n.1895G=
XR_934023.2:n.1916G=
NM_000018.4:c.1934G= MANE Select NP_000009.1:p.Gly645=
NM_001033859.3:c.1868G= NP_001029031.1:p.Gly623=
NM_001270447.2:c.2003G= NP_001257376.1:p.Gly668=
NM_001270448.2:c.1706G= NP_001257377.1:p.Gly569=