Canonical Allele Identifier: CA397725670
Gene: ACADVL HGNC NCBI

Linked Data

gnomAD v4: 17-7224653-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224653C>A , CM000679.2:g.7224653C>A GRCh38
NC_000017.10:g.7127972C>A , CM000679.1:g.7127972C>A GRCh37
NC_000017.9:g.7068696C>A NCBI36
NG_007975.1:g.9820C>A
NG_008391.2:g.398G>T
NG_033038.1:g.14892G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000356839.10:c.1690C>A MANE Select ENSP00000349297.5:p.Leu564Met
ENST00000322910.9:c.*1645C>A ENSP00000325395.5:n.*1645C>A
ENST00000350303.9:c.1624C>A ENSP00000344152.5:p.Leu542Met
ENST00000356839.9:c.1690C>A ENSP00000349297.5:p.Leu564Met
ENST00000542255.6:c.537-62C>A
ENST00000543245.6:c.1759C>A ENSP00000438689.2:p.Leu587Met
ENST00000578033.1:n.21C>A
ENST00000578319.5:n.271C>A
ENST00000578711.1:n.1149C>A
ENST00000578809.5:n.262C>A
ENST00000579425.5:n.806C>A
ENST00000579546.1:c.425C>A
ENST00000582450.1:n.287C>A
ENST00000583074.5:n.300-62C>A
ENST00000583848.5:c.65-9C>A ENSP00000466487.1:n.65-9C>A
ENST00000583850.5:n.461C>A
ENST00000583858.5:c.621C>A
ENST00000585203.6:n.881C>A
NM_000018.3:c.1690C>A NP_000009.1:p.Leu564Met
NM_001033859.2:c.1624C>A NP_001029031.1:p.Leu542Met
NM_001270447.1:c.1759C>A NP_001257376.1:p.Leu587Met
NM_001270448.1:c.1462C>A NP_001257377.1:p.Leu488Met
XM_006721516.2:c.1679-62C>A XP_006721579.2:n.1679-62C>A
XM_011523829.1:c.1577-62C>A XP_011522131.1:n.1577-62C>A
XM_011523830.1:c.1588C>A XP_011522132.1:p.Leu530Met
XR_934021.1:n.1793C>A
XR_934022.1:n.1699C>A
XR_934023.1:n.1688-62C>A
XM_006721516.3:c.1679-62C>A XP_006721579.2:n.1679-62C>A
XM_011523829.2:c.1577-62C>A XP_011522131.1:n.1577-62C>A
XM_011523830.2:c.1588C>A XP_011522132.1:p.Leu530Met
XM_024450741.1:c.1678C>A XP_024306509.1:p.Leu560Met
XR_934021.2:n.1745C>A
XR_934022.2:n.1651C>A
XR_934023.2:n.1640-62C>A
NM_000018.4:c.1690C>A MANE Select NP_000009.1:p.Leu564Met
NM_001033859.3:c.1624C>A NP_001029031.1:p.Leu542Met
NM_001270447.2:c.1759C>A NP_001257376.1:p.Leu587Met
NM_001270448.2:c.1462C>A NP_001257377.1:p.Leu488Met