Canonical Allele Identifier: CA397724586
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223664T>A , CM000679.2:g.7223664T>A GRCh38
NC_000017.10:g.7126983T>A , CM000679.1:g.7126983T>A GRCh37
NC_000017.9:g.7067707T>A NCBI36
NG_007975.1:g.8831T>A
NG_008391.2:g.1387A>T
NG_033038.1:g.15881A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1203T>A MANE Select ENSP00000349297.5:p.Ser401Arg
ENST00000322910.9:c.*1158T>A ENSP00000325395.5:n.*1158T>A
ENST00000350303.9:c.1137T>A ENSP00000344152.5:p.Ser379Arg
ENST00000356839.9:c.1203T>A ENSP00000349297.5:p.Ser401Arg
ENST00000542255.6:c.61T>A
ENST00000543245.6:c.1272T>A ENSP00000438689.2:p.Ser424Arg
ENST00000578579.2:n.374T>A
ENST00000578711.1:n.160T>A
ENST00000578824.5:n.619T>A
ENST00000579425.5:n.227T>A
ENST00000579546.1:c.40T>A
ENST00000583858.5:c.232T>A
ENST00000585203.6:n.411T>A
NM_000018.3:c.1203T>A NP_000009.1:p.Ser401Arg
NM_001033859.2:c.1137T>A NP_001029031.1:p.Ser379Arg
NM_001270447.1:c.1272T>A NP_001257376.1:p.Ser424Arg
NM_001270448.1:c.975T>A NP_001257377.1:p.Ser325Arg
XM_006721516.2:c.1203T>A XP_006721579.2:p.Ser401Arg
XM_011523829.1:c.1203T>A XP_011522131.1:p.Ser401Arg
XM_011523830.1:c.1203T>A XP_011522132.1:p.Ser401Arg
XR_934021.1:n.1310T>A
XR_934022.1:n.1310T>A
XR_934023.1:n.1310T>A
XM_006721516.3:c.1203T>A XP_006721579.2:p.Ser401Arg
XM_011523829.2:c.1203T>A XP_011522131.1:p.Ser401Arg
XM_011523830.2:c.1203T>A XP_011522132.1:p.Ser401Arg
XM_024450741.1:c.1203T>A XP_024306509.1:p.Ser401Arg
XR_934021.2:n.1262T>A
XR_934022.2:n.1262T>A
XR_934023.2:n.1262T>A
NM_000018.4:c.1203T>A MANE Select NP_000009.1:p.Ser401Arg
NM_001033859.3:c.1137T>A NP_001029031.1:p.Ser379Arg
NM_001270447.2:c.1272T>A NP_001257376.1:p.Ser424Arg
NM_001270448.2:c.975T>A NP_001257377.1:p.Ser325Arg