Canonical Allele Identifier: CA397725569
Gene: ACADVL HGNC NCBI

Linked Data

dbSNP Id: rs2071384555
gnomAD v3: 17-7224525-C-A
gnomAD v4: 17-7224525-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224525C>A , CM000679.2:g.7224525C>A GRCh38
NC_000017.10:g.7127844C>A , CM000679.1:g.7127844C>A GRCh37
NC_000017.9:g.7068568C>A NCBI36
NG_007975.1:g.9692C>A
NG_008391.2:g.526G>T
NG_033038.1:g.15020G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1651C>A MANE Select ENSP00000349297.5:p.Leu551Met
ENST00000322910.9:c.*1606C>A ENSP00000325395.5:n.*1606C>A
ENST00000350303.9:c.1585C>A ENSP00000344152.5:p.Leu529Met
ENST00000356839.9:c.1651C>A ENSP00000349297.5:p.Leu551Met
ENST00000542255.6:c.509C>A
ENST00000543245.6:c.1720C>A ENSP00000438689.2:p.Leu574Met
ENST00000578319.5:n.232C>A
ENST00000578711.1:n.1021C>A
ENST00000578809.5:n.223C>A
ENST00000579391.1:n.255C>A
ENST00000579425.5:n.767C>A
ENST00000579546.1:c.386C>A
ENST00000582450.1:n.159C>A
ENST00000583074.5:n.272C>A
ENST00000583848.5:c.37C>A ENSP00000466487.1:p.Leu13Met
ENST00000583850.5:n.422C>A
ENST00000583858.5:c.582C>A
ENST00000585203.6:n.842C>A
NM_000018.3:c.1651C>A NP_000009.1:p.Leu551Met
NM_001033859.2:c.1585C>A NP_001029031.1:p.Leu529Met
NM_001270447.1:c.1720C>A NP_001257376.1:p.Leu574Met
NM_001270448.1:c.1423C>A NP_001257377.1:p.Leu475Met
XM_006721516.2:c.1651C>A XP_006721579.2:p.Leu551Met
XM_011523829.1:c.1549C>A XP_011522131.1:p.Leu517Met
XM_011523830.1:c.1549C>A XP_011522132.1:p.Leu517Met
XR_934021.1:n.1754C>A
XR_934022.1:n.1660C>A
XR_934023.1:n.1660C>A
XM_006721516.3:c.1651C>A XP_006721579.2:p.Leu551Met
XM_011523829.2:c.1549C>A XP_011522131.1:p.Leu517Met
XM_011523830.2:c.1549C>A XP_011522132.1:p.Leu517Met
XM_024450741.1:c.1639C>A XP_024306509.1:p.Leu547Met
XR_934021.2:n.1706C>A
XR_934022.2:n.1612C>A
XR_934023.2:n.1612C>A
NM_000018.4:c.1651C>A MANE Select NP_000009.1:p.Leu551Met
NM_001033859.3:c.1585C>A NP_001029031.1:p.Leu529Met
NM_001270447.2:c.1720C>A NP_001257376.1:p.Leu574Met
NM_001270448.2:c.1423C>A NP_001257377.1:p.Leu475Met