Canonical Allele Identifier: CA8338133
Gene: ACADVL HGNC NCBI

Linked Data

dbSNP Id: rs758069646
gnomAD v2: 17-7127531-C-G
gnomAD v4: 17-7224212-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224212C>G , CM000679.2:g.7224212C>G GRCh38
NC_000017.10:g.7127531C>G , CM000679.1:g.7127531C>G GRCh37
NC_000017.9:g.7068255C>G NCBI36
NG_007975.1:g.9379C>G
NG_008391.2:g.839G>C
NG_033038.1:g.15333G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1501C>G MANE Select ENSP00000349297.5:p.Leu501Val
ENST00000322910.9:c.*1456C>G ENSP00000325395.5:n.*1456C>G
ENST00000350303.9:c.1435C>G ENSP00000344152.5:p.Leu479Val
ENST00000356839.9:c.1501C>G ENSP00000349297.5:p.Leu501Val
ENST00000542255.6:c.359C>G
ENST00000543245.6:c.1570C>G ENSP00000438689.2:p.Leu524Val
ENST00000578711.1:n.708C>G
ENST00000579391.1:n.109C>G
ENST00000579425.5:n.617C>G
ENST00000579546.1:c.272-109C>G
ENST00000579894.5:n.288C>G
ENST00000583074.5:n.154-109C>G
ENST00000583850.5:n.276C>G
ENST00000583858.5:c.464-109C>G
ENST00000585203.6:n.692C>G
NM_000018.3:c.1501C>G NP_000009.1:p.Leu501Val
NM_001033859.2:c.1435C>G NP_001029031.1:p.Leu479Val
NM_001270447.1:c.1570C>G NP_001257376.1:p.Leu524Val
NM_001270448.1:c.1273C>G NP_001257377.1:p.Leu425Val
XM_006721516.2:c.1501C>G XP_006721579.2:p.Leu501Val
XM_011523829.1:c.1435-109C>G XP_011522131.1:n.1435-109C>G
XM_011523830.1:c.1435-109C>G XP_011522132.1:n.1435-109C>G
XR_934021.1:n.1608C>G
XR_934022.1:n.1542-109C>G
XR_934023.1:n.1542-109C>G
XM_006721516.3:c.1501C>G XP_006721579.2:p.Leu501Val
XM_011523829.2:c.1435-109C>G XP_011522131.1:n.1435-109C>G
XM_011523830.2:c.1435-109C>G XP_011522132.1:n.1435-109C>G
XM_024450741.1:c.1435-109C>G XP_024306509.1:n.1435-109C>G
XR_934021.2:n.1560C>G
XR_934022.2:n.1494-109C>G
XR_934023.2:n.1494-109C>G
NM_000018.4:c.1501C>G MANE Select NP_000009.1:p.Leu501Val
NM_001033859.3:c.1435C>G NP_001029031.1:p.Leu479Val
NM_001270447.2:c.1570C>G NP_001257376.1:p.Leu524Val
NM_001270448.2:c.1273C>G NP_001257377.1:p.Leu425Val