Canonical Allele Identifier: CA2245713138
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224137C= , CM000679.2:g.7224137C= GRCh38
NC_000017.10:g.7127456C= , CM000679.1:g.7127456C= GRCh37
NC_000017.9:g.7068180C= NCBI36
NG_007975.1:g.9304C=
NG_008391.2:g.914G=
NG_033038.1:g.15408G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1435-9C= MANE Select ENSP00000349297.5:n.1435-9C=
ENST00000322910.9:c.*1390-9C= ENSP00000325395.5:n.*1390-9C=
ENST00000350303.9:c.1369-9C= ENSP00000344152.5:n.1369-9C=
ENST00000356839.9:c.1435-9C= ENSP00000349297.5:n.1435-9C=
ENST00000542255.6:c.293-9C=
ENST00000543245.6:c.1504-9C= ENSP00000438689.2:n.1504-9C=
ENST00000578711.1:n.633C=
ENST00000579391.1:n.34C=
ENST00000579425.5:n.551-9C=
ENST00000579546.1:c.271+68C=
ENST00000579894.5:n.213C=
ENST00000583074.5:n.153+68C=
ENST00000583850.5:n.210-9C=
ENST00000583858.5:c.463+68C=
ENST00000585203.6:n.626-9C=
NM_000018.3:c.1435-9C= NP_000009.1:n.1435-9C=
NM_001033859.2:c.1369-9C= NP_001029031.1:n.1369-9C=
NM_001270447.1:c.1504-9C= NP_001257376.1:n.1504-9C=
NM_001270448.1:c.1207-9C= NP_001257377.1:n.1207-9C=
XM_006721516.2:c.1435-9C= XP_006721579.2:n.1435-9C=
XM_011523829.1:c.1434+68C= XP_011522131.1:n.1434+68C=
XM_011523830.1:c.1434+68C= XP_011522132.1:n.1434+68C=
XR_934021.1:n.1542-9C=
XR_934022.1:n.1541+68C=
XR_934023.1:n.1541+68C=
XM_006721516.3:c.1435-9C= XP_006721579.2:n.1435-9C=
XM_011523829.2:c.1434+68C= XP_011522131.1:n.1434+68C=
XM_011523830.2:c.1434+68C= XP_011522132.1:n.1434+68C=
XM_024450741.1:c.1434+68C= XP_024306509.1:n.1434+68C=
XR_934021.2:n.1494-9C=
XR_934022.2:n.1493+68C=
XR_934023.2:n.1493+68C=
NM_000018.4:c.1435-9C= MANE Select NP_000009.1:n.1435-9C=
NM_001033859.3:c.1369-9C= NP_001029031.1:n.1369-9C=
NM_001270447.2:c.1504-9C= NP_001257376.1:n.1504-9C=
NM_001270448.2:c.1207-9C= NP_001257377.1:n.1207-9C=