Canonical Allele Identifier: CA397722325
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7220605A>C , CM000679.2:g.7220605A>C GRCh38
NC_000017.10:g.7123924A>C , CM000679.1:g.7123924A>C GRCh37
NC_000017.9:g.7064648A>C NCBI36
NG_007975.1:g.5772A>C
NG_008391.2:g.4446T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.206A>C MANE Select ENSP00000349297.5:p.Glu69Ala
ENST00000322910.9:c.*161A>C ENSP00000325395.5:n.*161A>C
ENST00000350303.9:c.140A>C ENSP00000344152.5:p.Glu47Ala
ENST00000356839.9:c.206A>C ENSP00000349297.5:p.Glu69Ala
ENST00000543245.6:c.275A>C ENSP00000438689.2:p.Glu92Ala
ENST00000577191.5:n.283A>C
ENST00000577433.5:n.414A>C
ENST00000577857.5:n.229-161A>C
ENST00000578269.5:n.653A>C
ENST00000578421.1:n.414A>C
ENST00000579286.5:n.387A>C
ENST00000579886.2:c.201+79A>C ENSP00000463246.1:n.201+79A>C
ENST00000580263.5:n.370A>C
ENST00000581562.5:n.253A>C
ENST00000582056.5:n.296A>C
ENST00000582166.1:n.94A>C
ENST00000582356.5:n.405A>C
ENST00000583312.5:c.206A>C ENSP00000467920.1:p.Glu69Ala
ENST00000584103.5:c.206A>C ENSP00000465353.1:p.Glu69Ala
NM_000018.3:c.206A>C NP_000009.1:p.Glu69Ala
NM_001033859.2:c.140A>C NP_001029031.1:p.Glu47Ala
NM_001270447.1:c.275A>C NP_001257376.1:p.Glu92Ala
NM_001270448.1:c.-23A>C NP_001257377.1:n.-23A>C
XM_006721516.2:c.206A>C XP_006721579.2:p.Glu69Ala
XM_011523829.1:c.206A>C XP_011522131.1:p.Glu69Ala
XM_011523830.1:c.206A>C XP_011522132.1:p.Glu69Ala
XR_934021.1:n.313A>C
XR_934022.1:n.313A>C
XR_934023.1:n.313A>C
XM_006721516.3:c.206A>C XP_006721579.2:p.Glu69Ala
XM_011523829.2:c.206A>C XP_011522131.1:p.Glu69Ala
XM_011523830.2:c.206A>C XP_011522132.1:p.Glu69Ala
XM_024450741.1:c.206A>C XP_024306509.1:p.Glu69Ala
XR_934021.2:n.265A>C
XR_934022.2:n.265A>C
XR_934023.2:n.265A>C
NM_000018.4:c.206A>C MANE Select NP_000009.1:p.Glu69Ala
NM_001033859.3:c.140A>C NP_001029031.1:p.Glu47Ala
NM_001270447.2:c.275A>C NP_001257376.1:p.Glu92Ala
NM_001270448.2:c.-23A>C NP_001257377.1:n.-23A>C