Canonical Allele Identifier: CA2245712806
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224058C= , CM000679.2:g.7224058C= GRCh38
NC_000017.10:g.7127377C= , CM000679.1:g.7127377C= GRCh37
NC_000017.9:g.7068101C= NCBI36
NG_007975.1:g.9225C=
NG_008391.2:g.993G=
NG_033038.1:g.15487G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1423C= MANE Select ENSP00000349297.5:p.Gln475=
ENST00000322910.9:c.*1378C= ENSP00000325395.5:n.*1378C=
ENST00000350303.9:c.1357C= ENSP00000344152.5:p.Gln453=
ENST00000356839.9:c.1423C= ENSP00000349297.5:p.Gln475=
ENST00000542255.6:c.281C=
ENST00000543245.6:c.1492C= ENSP00000438689.2:p.Gln498=
ENST00000578711.1:n.554C=
ENST00000579425.5:n.539C=
ENST00000579546.1:c.260C=
ENST00000579894.5:n.134C=
ENST00000583074.5:n.142C=
ENST00000583850.5:n.198C=
ENST00000583858.5:c.452C=
ENST00000585203.6:n.614C=
NM_000018.3:c.1423C= NP_000009.1:p.Gln475=
NM_001033859.2:c.1357C= NP_001029031.1:p.Gln453=
NM_001270447.1:c.1492C= NP_001257376.1:p.Gln498=
NM_001270448.1:c.1195C= NP_001257377.1:p.Gln399=
XM_006721516.2:c.1423C= XP_006721579.2:p.Gln475=
XM_011523829.1:c.1423C= XP_011522131.1:p.Gln475=
XM_011523830.1:c.1423C= XP_011522132.1:p.Gln475=
XR_934021.1:n.1530C=
XR_934022.1:n.1530C=
XR_934023.1:n.1530C=
XM_006721516.3:c.1423C= XP_006721579.2:p.Gln475=
XM_011523829.2:c.1423C= XP_011522131.1:p.Gln475=
XM_011523830.2:c.1423C= XP_011522132.1:p.Gln475=
XM_024450741.1:c.1423C= XP_024306509.1:p.Gln475=
XR_934021.2:n.1482C=
XR_934022.2:n.1482C=
XR_934023.2:n.1482C=
NM_000018.4:c.1423C= MANE Select NP_000009.1:p.Gln475=
NM_001033859.3:c.1357C= NP_001029031.1:p.Gln453=
NM_001270447.2:c.1492C= NP_001257376.1:p.Gln498=
NM_001270448.2:c.1195C= NP_001257377.1:p.Gln399=