Canonical Allele Identifier: CA2245698527
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7220611A= , CM000679.2:g.7220611A= GRCh38
NC_000017.10:g.7123930A= , CM000679.1:g.7123930A= GRCh37
NC_000017.9:g.7064654A= NCBI36
NG_007975.1:g.5778A=
NG_008391.2:g.4440T=

Transcript Alleles

HGVS Amino-acid change
ENST00000356839.10:c.212A= MANE Select ENSP00000349297.5:p.Lys71=
ENST00000322910.9:c.*167A= ENSP00000325395.5:n.*167A=
ENST00000350303.9:c.146A= ENSP00000344152.5:p.Lys49=
ENST00000356839.9:c.212A= ENSP00000349297.5:p.Lys71=
ENST00000543245.6:c.281A= ENSP00000438689.2:p.Lys94=
ENST00000577191.5:n.289A=
ENST00000577433.5:n.420A=
ENST00000577857.5:n.229-155A=
ENST00000578269.5:n.659A=
ENST00000578421.1:n.420A=
ENST00000579286.5:n.393A=
ENST00000579886.2:c.201+85A= ENSP00000463246.1:n.201+85A=
ENST00000580263.5:n.376A=
ENST00000581562.5:n.259A=
ENST00000582056.5:n.302A=
ENST00000582166.1:n.100A=
ENST00000582356.5:n.411A=
ENST00000583312.5:c.212A= ENSP00000467920.1:p.Lys71=
ENST00000584103.5:c.212A= ENSP00000465353.1:p.Lys71=
NM_000018.3:c.212A= NP_000009.1:p.Lys71=
NM_001033859.2:c.146A= NP_001029031.1:p.Lys49=
NM_001270447.1:c.281A= NP_001257376.1:p.Lys94=
NM_001270448.1:c.-17A= NP_001257377.1:n.-17A=
XM_006721516.2:c.212A= XP_006721579.2:p.Lys71=
XM_011523829.1:c.212A= XP_011522131.1:p.Lys71=
XM_011523830.1:c.212A= XP_011522132.1:p.Lys71=
XR_934021.1:n.319A=
XR_934022.1:n.319A=
XR_934023.1:n.319A=
XM_006721516.3:c.212A= XP_006721579.2:p.Lys71=
XM_011523829.2:c.212A= XP_011522131.1:p.Lys71=
XM_011523830.2:c.212A= XP_011522132.1:p.Lys71=
XM_024450741.1:c.212A= XP_024306509.1:p.Lys71=
XR_934021.2:n.271A=
XR_934022.2:n.271A=
XR_934023.2:n.271A=
NM_000018.4:c.212A= MANE Select NP_000009.1:p.Lys71=
NM_001033859.3:c.146A= NP_001029031.1:p.Lys49=
NM_001270447.2:c.281A= NP_001257376.1:p.Lys94=
NM_001270448.2:c.-17A= NP_001257377.1:n.-17A=