Canonical Allele Identifier: CA2245698515
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7220608C= , CM000679.2:g.7220608C= GRCh38
NC_000017.10:g.7123927C= , CM000679.1:g.7123927C= GRCh37
NC_000017.9:g.7064651C= NCBI36
NG_007975.1:g.5775C=
NG_008391.2:g.4443G=

Transcript Alleles

HGVS Amino-acid change
ENST00000356839.10:c.209C= MANE Select ENSP00000349297.5:p.Ser70=
ENST00000322910.9:c.*164C= ENSP00000325395.5:n.*164C=
ENST00000350303.9:c.143C= ENSP00000344152.5:p.Ser48=
ENST00000356839.9:c.209C= ENSP00000349297.5:p.Ser70=
ENST00000543245.6:c.278C= ENSP00000438689.2:p.Ser93=
ENST00000577191.5:n.286C=
ENST00000577433.5:n.417C=
ENST00000577857.5:n.229-158C=
ENST00000578269.5:n.656C=
ENST00000578421.1:n.417C=
ENST00000579286.5:n.390C=
ENST00000579886.2:c.201+82C= ENSP00000463246.1:n.201+82C=
ENST00000580263.5:n.373C=
ENST00000581562.5:n.256C=
ENST00000582056.5:n.299C=
ENST00000582166.1:n.97C=
ENST00000582356.5:n.408C=
ENST00000583312.5:c.209C= ENSP00000467920.1:p.Ser70=
ENST00000584103.5:c.209C= ENSP00000465353.1:p.Ser70=
NM_000018.3:c.209C= NP_000009.1:p.Ser70=
NM_001033859.2:c.143C= NP_001029031.1:p.Ser48=
NM_001270447.1:c.278C= NP_001257376.1:p.Ser93=
NM_001270448.1:c.-20C= NP_001257377.1:n.-20C=
XM_006721516.2:c.209C= XP_006721579.2:p.Ser70=
XM_011523829.1:c.209C= XP_011522131.1:p.Ser70=
XM_011523830.1:c.209C= XP_011522132.1:p.Ser70=
XR_934021.1:n.316C=
XR_934022.1:n.316C=
XR_934023.1:n.316C=
XM_006721516.3:c.209C= XP_006721579.2:p.Ser70=
XM_011523829.2:c.209C= XP_011522131.1:p.Ser70=
XM_011523830.2:c.209C= XP_011522132.1:p.Ser70=
XM_024450741.1:c.209C= XP_024306509.1:p.Ser70=
XR_934021.2:n.268C=
XR_934022.2:n.268C=
XR_934023.2:n.268C=
NM_000018.4:c.209C= MANE Select NP_000009.1:p.Ser70=
NM_001033859.3:c.143C= NP_001029031.1:p.Ser48=
NM_001270447.2:c.278C= NP_001257376.1:p.Ser93=
NM_001270448.2:c.-20C= NP_001257377.1:n.-20C=