Canonical Allele Identifier: CA397724731
Gene: ACADVL HGNC NCBI

Linked Data

ClinVar Variation Id: 582635
ClinVar RCV Id: RCV000706755
dbSNP Id: rs1451455641
gnomAD v2: 17-7127048-C-T
gnomAD v4: 17-7223729-C-T
COSMIC: COSM983828

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223729C>T , CM000679.2:g.7223729C>T GRCh38
NC_000017.10:g.7127048C>T , CM000679.1:g.7127048C>T GRCh37
NC_000017.9:g.7067772C>T NCBI36
NG_007975.1:g.8896C>T
NG_008391.2:g.1322G>A
NG_033038.1:g.15816G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1268C>T MANE Select ENSP00000349297.5:p.Ser423Leu
ENST00000322910.9:c.*1223C>T ENSP00000325395.5:n.*1223C>T
ENST00000350303.9:c.1202C>T ENSP00000344152.5:p.Ser401Leu
ENST00000356839.9:c.1268C>T ENSP00000349297.5:p.Ser423Leu
ENST00000542255.6:c.126C>T
ENST00000543245.6:c.1337C>T ENSP00000438689.2:p.Ser446Leu
ENST00000578579.2:n.439C>T
ENST00000578711.1:n.225C>T
ENST00000578824.5:n.684C>T
ENST00000579425.5:n.292C>T
ENST00000579546.1:c.105C>T
ENST00000583850.5:n.43C>T
ENST00000583858.5:c.297C>T
ENST00000585203.6:n.476C>T
NM_000018.3:c.1268C>T NP_000009.1:p.Ser423Leu
NM_001033859.2:c.1202C>T NP_001029031.1:p.Ser401Leu
NM_001270447.1:c.1337C>T NP_001257376.1:p.Ser446Leu
NM_001270448.1:c.1040C>T NP_001257377.1:p.Ser347Leu
XM_006721516.2:c.1268C>T XP_006721579.2:p.Ser423Leu
XM_011523829.1:c.1268C>T XP_011522131.1:p.Ser423Leu
XM_011523830.1:c.1268C>T XP_011522132.1:p.Ser423Leu
XR_934021.1:n.1375C>T
XR_934022.1:n.1375C>T
XR_934023.1:n.1375C>T
XM_006721516.3:c.1268C>T XP_006721579.2:p.Ser423Leu
XM_011523829.2:c.1268C>T XP_011522131.1:p.Ser423Leu
XM_011523830.2:c.1268C>T XP_011522132.1:p.Ser423Leu
XM_024450741.1:c.1268C>T XP_024306509.1:p.Ser423Leu
XR_934021.2:n.1327C>T
XR_934022.2:n.1327C>T
XR_934023.2:n.1327C>T
NM_000018.4:c.1268C>T MANE Select NP_000009.1:p.Ser423Leu
NM_001033859.3:c.1202C>T NP_001029031.1:p.Ser401Leu
NM_001270447.2:c.1337C>T NP_001257376.1:p.Ser446Leu
NM_001270448.2:c.1040C>T NP_001257377.1:p.Ser347Leu