Canonical Allele Identifier: CA2245698922
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7220773C= , CM000679.2:g.7220773C= GRCh38
NC_000017.10:g.7124092C= , CM000679.1:g.7124092C= GRCh37
NC_000017.9:g.7064816C= NCBI36
NG_007975.1:g.5940C=
NG_008391.2:g.4278G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.285C= MANE Select ENSP00000349297.5:p.Asn95=
ENST00000322910.9:c.*240C= ENSP00000325395.5:n.*240C=
ENST00000350303.9:c.219C= ENSP00000344152.5:p.Asn73=
ENST00000356839.9:c.285C= ENSP00000349297.5:p.Asn95=
ENST00000543245.6:c.354C= ENSP00000438689.2:p.Asn118=
ENST00000577191.5:n.362C=
ENST00000577433.5:n.493C=
ENST00000577857.5:n.236C=
ENST00000579286.5:n.466C=
ENST00000579886.2:c.202-172C= ENSP00000463246.1:n.202-172C=
ENST00000580263.5:n.538C=
ENST00000580365.1:n.16C=
ENST00000581562.5:n.332C=
ENST00000582056.5:n.375C=
ENST00000582166.1:n.173C=
ENST00000582356.5:n.484C=
ENST00000583312.5:c.285C= ENSP00000467920.1:p.Asn95=
ENST00000584103.5:c.285C= ENSP00000465353.1:p.Asn95=
NM_000018.3:c.285C= NP_000009.1:p.Asn95=
NM_001033859.2:c.219C= NP_001029031.1:p.Asn73=
NM_001270447.1:c.354C= NP_001257376.1:p.Asn118=
NM_001270448.1:c.57C= NP_001257377.1:p.Asn19=
XM_006721516.2:c.285C= XP_006721579.2:p.Asn95=
XM_011523829.1:c.285C= XP_011522131.1:p.Asn95=
XM_011523830.1:c.285C= XP_011522132.1:p.Asn95=
XR_934021.1:n.392C=
XR_934022.1:n.392C=
XR_934023.1:n.392C=
XM_006721516.3:c.285C= XP_006721579.2:p.Asn95=
XM_011523829.2:c.285C= XP_011522131.1:p.Asn95=
XM_011523830.2:c.285C= XP_011522132.1:p.Asn95=
XM_024450741.1:c.285C= XP_024306509.1:p.Asn95=
XR_934021.2:n.344C=
XR_934022.2:n.344C=
XR_934023.2:n.344C=
NM_000018.4:c.285C= MANE Select NP_000009.1:p.Asn95=
NM_001033859.3:c.219C= NP_001029031.1:p.Asn73=
NM_001270447.2:c.354C= NP_001257376.1:p.Asn118=
NM_001270448.2:c.57C= NP_001257377.1:p.Asn19=