Canonical Allele Identifier: CA397724862
Gene: ACADVL HGNC NCBI

Linked Data

ClinVar Variation Id: 932764
ClinVar RCV Id: RCV001200704
dbSNP Id: rs2071346777
gnomAD v4: 17-7223864-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223864G>A , CM000679.2:g.7223864G>A GRCh38
NC_000017.10:g.7127183G>A , CM000679.1:g.7127183G>A GRCh37
NC_000017.9:g.7067907G>A NCBI36
NG_007975.1:g.9031G>A
NG_008391.2:g.1187C>T
NG_033038.1:g.15681C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1321G>A MANE Select ENSP00000349297.5:p.Gly441Ser
ENST00000322910.9:c.*1276G>A ENSP00000325395.5:n.*1276G>A
ENST00000350303.9:c.1255G>A ENSP00000344152.5:p.Gly419Ser
ENST00000356839.9:c.1321G>A ENSP00000349297.5:p.Gly441Ser
ENST00000542255.6:c.179G>A
ENST00000543245.6:c.1390G>A ENSP00000438689.2:p.Gly464Ser
ENST00000578711.1:n.360G>A
ENST00000579425.5:n.345G>A
ENST00000579546.1:c.158G>A
ENST00000583074.5:n.40G>A
ENST00000583850.5:n.96G>A
ENST00000583858.5:c.350G>A
ENST00000585203.6:n.523+6G>A
NM_000018.3:c.1321G>A NP_000009.1:p.Gly441Ser
NM_001033859.2:c.1255G>A NP_001029031.1:p.Gly419Ser
NM_001270447.1:c.1390G>A NP_001257376.1:p.Gly464Ser
NM_001270448.1:c.1093G>A NP_001257377.1:p.Gly365Ser
XM_006721516.2:c.1321G>A XP_006721579.2:p.Gly441Ser
XM_011523829.1:c.1321G>A XP_011522131.1:p.Gly441Ser
XM_011523830.1:c.1321G>A XP_011522132.1:p.Gly441Ser
XR_934021.1:n.1428G>A
XR_934022.1:n.1428G>A
XR_934023.1:n.1428G>A
XM_006721516.3:c.1321G>A XP_006721579.2:p.Gly441Ser
XM_011523829.2:c.1321G>A XP_011522131.1:p.Gly441Ser
XM_011523830.2:c.1321G>A XP_011522132.1:p.Gly441Ser
XM_024450741.1:c.1321G>A XP_024306509.1:p.Gly441Ser
XR_934021.2:n.1380G>A
XR_934022.2:n.1380G>A
XR_934023.2:n.1380G>A
NM_000018.4:c.1321G>A MANE Select NP_000009.1:p.Gly441Ser
NM_001033859.3:c.1255G>A NP_001029031.1:p.Gly419Ser
NM_001270447.2:c.1390G>A NP_001257376.1:p.Gly464Ser
NM_001270448.2:c.1093G>A NP_001257377.1:p.Gly365Ser