Canonical Allele Identifier: CA2635783561
Gene: ACADVL HGNC NCBI

Linked Data

ClinVar Variation Id: 2879274
ClinVar RCV Id: RCV003600236
gnomAD v4: 17-7224141-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224141C>T , CM000679.2:g.7224141C>T GRCh38
NC_000017.10:g.7127460C>T , CM000679.1:g.7127460C>T GRCh37
NC_000017.9:g.7068184C>T NCBI36
NG_007975.1:g.9308C>T
NG_008391.2:g.910G>A
NG_033038.1:g.15404G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1435-5C>T MANE Select ENSP00000349297.5:n.1435-5C>T
ENST00000322910.9:c.*1390-5C>T ENSP00000325395.5:n.*1390-5C>T
ENST00000350303.9:c.1369-5C>T ENSP00000344152.5:n.1369-5C>T
ENST00000356839.9:c.1435-5C>T ENSP00000349297.5:n.1435-5C>T
ENST00000542255.6:c.293-5C>T
ENST00000543245.6:c.1504-5C>T ENSP00000438689.2:n.1504-5C>T
ENST00000578711.1:n.637C>T
ENST00000579391.1:n.38C>T
ENST00000579425.5:n.551-5C>T
ENST00000579546.1:c.271+72C>T
ENST00000579894.5:n.217C>T
ENST00000583074.5:n.153+72C>T
ENST00000583850.5:n.210-5C>T
ENST00000583858.5:c.463+72C>T
ENST00000585203.6:n.626-5C>T
NM_000018.3:c.1435-5C>T NP_000009.1:n.1435-5C>T
NM_001033859.2:c.1369-5C>T NP_001029031.1:n.1369-5C>T
NM_001270447.1:c.1504-5C>T NP_001257376.1:n.1504-5C>T
NM_001270448.1:c.1207-5C>T NP_001257377.1:n.1207-5C>T
XM_006721516.2:c.1435-5C>T XP_006721579.2:n.1435-5C>T
XM_011523829.1:c.1434+72C>T XP_011522131.1:n.1434+72C>T
XM_011523830.1:c.1434+72C>T XP_011522132.1:n.1434+72C>T
XR_934021.1:n.1542-5C>T
XR_934022.1:n.1541+72C>T
XR_934023.1:n.1541+72C>T
XM_006721516.3:c.1435-5C>T XP_006721579.2:n.1435-5C>T
XM_011523829.2:c.1434+72C>T XP_011522131.1:n.1434+72C>T
XM_011523830.2:c.1434+72C>T XP_011522132.1:n.1434+72C>T
XM_024450741.1:c.1434+72C>T XP_024306509.1:n.1434+72C>T
XR_934021.2:n.1494-5C>T
XR_934022.2:n.1493+72C>T
XR_934023.2:n.1493+72C>T
NM_000018.4:c.1435-5C>T MANE Select NP_000009.1:n.1435-5C>T
NM_001033859.3:c.1369-5C>T NP_001029031.1:n.1369-5C>T
NM_001270447.2:c.1504-5C>T NP_001257376.1:n.1504-5C>T
NM_001270448.2:c.1207-5C>T NP_001257377.1:n.1207-5C>T