Canonical Allele Identifier: CA2245698909
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7220766T= , CM000679.2:g.7220766T= GRCh38
NC_000017.10:g.7124085T= , CM000679.1:g.7124085T= GRCh37
NC_000017.9:g.7064809T= NCBI36
NG_007975.1:g.5933T=
NG_008391.2:g.4285A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.278T= MANE Select ENSP00000349297.5:p.Val93=
ENST00000322910.9:c.*233T= ENSP00000325395.5:n.*233T=
ENST00000350303.9:c.212T= ENSP00000344152.5:p.Val71=
ENST00000356839.9:c.278T= ENSP00000349297.5:p.Val93=
ENST00000543245.6:c.347T= ENSP00000438689.2:p.Val116=
ENST00000577191.5:n.355T=
ENST00000577433.5:n.486T=
ENST00000577857.5:n.229T=
ENST00000579286.5:n.459T=
ENST00000579886.2:c.202-179T= ENSP00000463246.1:n.202-179T=
ENST00000580263.5:n.531T=
ENST00000580365.1:n.9T=
ENST00000581562.5:n.325T=
ENST00000582056.5:n.368T=
ENST00000582166.1:n.166T=
ENST00000582356.5:n.477T=
ENST00000583312.5:c.278T= ENSP00000467920.1:p.Val93=
ENST00000584103.5:c.278T= ENSP00000465353.1:p.Val93=
NM_000018.3:c.278T= NP_000009.1:p.Val93=
NM_001033859.2:c.212T= NP_001029031.1:p.Val71=
NM_001270447.1:c.347T= NP_001257376.1:p.Val116=
NM_001270448.1:c.50T= NP_001257377.1:p.Val17=
XM_006721516.2:c.278T= XP_006721579.2:p.Val93=
XM_011523829.1:c.278T= XP_011522131.1:p.Val93=
XM_011523830.1:c.278T= XP_011522132.1:p.Val93=
XR_934021.1:n.385T=
XR_934022.1:n.385T=
XR_934023.1:n.385T=
XM_006721516.3:c.278T= XP_006721579.2:p.Val93=
XM_011523829.2:c.278T= XP_011522131.1:p.Val93=
XM_011523830.2:c.278T= XP_011522132.1:p.Val93=
XM_024450741.1:c.278T= XP_024306509.1:p.Val93=
XR_934021.2:n.337T=
XR_934022.2:n.337T=
XR_934023.2:n.337T=
NM_000018.4:c.278T= MANE Select NP_000009.1:p.Val93=
NM_001033859.3:c.212T= NP_001029031.1:p.Val71=
NM_001270447.2:c.347T= NP_001257376.1:p.Val116=
NM_001270448.2:c.50T= NP_001257377.1:p.Val17=