Canonical Allele Identifier: CA2245699294
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221016A= , CM000679.2:g.7221016A= GRCh38
NC_000017.10:g.7124335A= , CM000679.1:g.7124335A= GRCh37
NC_000017.9:g.7065059A= NCBI36
NG_007975.1:g.6183A=
NG_008391.2:g.4035T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.435A= MANE Select ENSP00000349297.5:p.Gln145=
ENST00000322910.9:c.*390A= ENSP00000325395.5:n.*390A=
ENST00000350303.9:c.369A= ENSP00000344152.5:p.Gln123=
ENST00000356839.9:c.435A= ENSP00000349297.5:p.Gln145=
ENST00000543245.6:c.504A= ENSP00000438689.2:p.Gln168=
ENST00000577191.5:n.512A=
ENST00000577433.5:n.643A=
ENST00000577857.5:n.293+186A=
ENST00000579286.5:n.616A=
ENST00000579886.2:c.273A= ENSP00000463246.1:p.Gln91=
ENST00000580365.1:n.166A=
ENST00000581378.5:c.134A=
ENST00000581562.5:n.482A=
ENST00000582056.5:n.618A=
ENST00000582166.1:n.416A=
ENST00000583312.5:c.435A= ENSP00000467920.1:p.Gln145=
ENST00000584103.5:c.468A= ENSP00000465353.1:p.Gln156=
NM_000018.3:c.435A= NP_000009.1:p.Gln145=
NM_001033859.2:c.369A= NP_001029031.1:p.Gln123=
NM_001270447.1:c.504A= NP_001257376.1:p.Gln168=
NM_001270448.1:c.207A= NP_001257377.1:p.Gln69=
XM_006721516.2:c.435A= XP_006721579.2:p.Gln145=
XM_011523829.1:c.435A= XP_011522131.1:p.Gln145=
XM_011523830.1:c.435A= XP_011522132.1:p.Gln145=
XR_934021.1:n.542A=
XR_934022.1:n.542A=
XR_934023.1:n.542A=
XM_006721516.3:c.435A= XP_006721579.2:p.Gln145=
XM_011523829.2:c.435A= XP_011522131.1:p.Gln145=
XM_011523830.2:c.435A= XP_011522132.1:p.Gln145=
XM_024450741.1:c.435A= XP_024306509.1:p.Gln145=
XR_934021.2:n.494A=
XR_934022.2:n.494A=
XR_934023.2:n.494A=
NM_000018.4:c.435A= MANE Select NP_000009.1:p.Gln145=
NM_001033859.3:c.369A= NP_001029031.1:p.Gln123=
NM_001270447.2:c.504A= NP_001257376.1:p.Gln168=
NM_001270448.2:c.207A= NP_001257377.1:p.Gln69=