Canonical Allele Identifier: CA397725299
Gene: ACADVL HGNC NCBI

Linked Data

dbSNP Id: rs2071366876
gnomAD v3: 17-7224233-C-G
gnomAD v4: 17-7224233-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224233C>G , CM000679.2:g.7224233C>G GRCh38
NC_000017.10:g.7127552C>G , CM000679.1:g.7127552C>G GRCh37
NC_000017.9:g.7068276C>G NCBI36
NG_007975.1:g.9400C>G
NG_008391.2:g.818G>C
NG_033038.1:g.15312G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1522C>G MANE Select ENSP00000349297.5:p.Gln508Glu
ENST00000322910.9:c.*1477C>G ENSP00000325395.5:n.*1477C>G
ENST00000350303.9:c.1456C>G ENSP00000344152.5:p.Gln486Glu
ENST00000356839.9:c.1522C>G ENSP00000349297.5:p.Gln508Glu
ENST00000542255.6:c.380C>G
ENST00000543245.6:c.1591C>G ENSP00000438689.2:p.Gln531Glu
ENST00000578319.5:n.17C>G
ENST00000578711.1:n.729C>G
ENST00000578809.5:n.17C>G
ENST00000579391.1:n.130C>G
ENST00000579425.5:n.638C>G
ENST00000579546.1:c.272-88C>G
ENST00000579894.5:n.309C>G
ENST00000583074.5:n.154-88C>G
ENST00000583850.5:n.297C>G
ENST00000583858.5:c.464-88C>G
ENST00000585203.6:n.713C>G
NM_000018.3:c.1522C>G NP_000009.1:p.Gln508Glu
NM_001033859.2:c.1456C>G NP_001029031.1:p.Gln486Glu
NM_001270447.1:c.1591C>G NP_001257376.1:p.Gln531Glu
NM_001270448.1:c.1294C>G NP_001257377.1:p.Gln432Glu
XM_006721516.2:c.1522C>G XP_006721579.2:p.Gln508Glu
XM_011523829.1:c.1435-88C>G XP_011522131.1:n.1435-88C>G
XM_011523830.1:c.1435-88C>G XP_011522132.1:n.1435-88C>G
XR_934021.1:n.1629C>G
XR_934022.1:n.1542-88C>G
XR_934023.1:n.1542-88C>G
XM_006721516.3:c.1522C>G XP_006721579.2:p.Gln508Glu
XM_011523829.2:c.1435-88C>G XP_011522131.1:n.1435-88C>G
XM_011523830.2:c.1435-88C>G XP_011522132.1:n.1435-88C>G
XM_024450741.1:c.1435-88C>G XP_024306509.1:n.1435-88C>G
XR_934021.2:n.1581C>G
XR_934022.2:n.1494-88C>G
XR_934023.2:n.1494-88C>G
NM_000018.4:c.1522C>G MANE Select NP_000009.1:p.Gln508Glu
NM_001033859.3:c.1456C>G NP_001029031.1:p.Gln486Glu
NM_001270447.2:c.1591C>G NP_001257376.1:p.Gln531Glu
NM_001270448.2:c.1294C>G NP_001257377.1:p.Gln432Glu