Canonical Allele Identifier: CA2245700405
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221661T= , CM000679.2:g.7221661T= GRCh38
NC_000017.10:g.7124980T= , CM000679.1:g.7124980T= GRCh37
NC_000017.9:g.7065704T= NCBI36
NG_007975.1:g.6828T=
NG_008391.2:g.3390A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.601T= MANE Select ENSP00000349297.5:p.Tyr201=
ENST00000322910.9:c.*556T= ENSP00000325395.5:n.*556T=
ENST00000350303.9:c.535T= ENSP00000344152.5:p.Tyr179=
ENST00000356839.9:c.601T= ENSP00000349297.5:p.Tyr201=
ENST00000543245.6:c.670T= ENSP00000438689.2:p.Tyr224=
ENST00000577191.5:n.678T=
ENST00000577857.5:n.417T=
ENST00000579286.5:n.782T=
ENST00000579886.2:c.439T= ENSP00000463246.1:p.Tyr147=
ENST00000580365.1:n.332T=
ENST00000581378.5:c.319T=
ENST00000581562.5:n.525-291T=
ENST00000583312.5:c.601T= ENSP00000467920.1:p.Tyr201=
ENST00000583760.1:n.383T=
NM_000018.3:c.601T= NP_000009.1:p.Tyr201=
NM_001033859.2:c.535T= NP_001029031.1:p.Tyr179=
NM_001270447.1:c.670T= NP_001257376.1:p.Tyr224=
NM_001270448.1:c.373T= NP_001257377.1:p.Tyr125=
XM_006721516.2:c.601T= XP_006721579.2:p.Tyr201=
XM_011523829.1:c.601T= XP_011522131.1:p.Tyr201=
XM_011523830.1:c.601T= XP_011522132.1:p.Tyr201=
XR_934021.1:n.708T=
XR_934022.1:n.708T=
XR_934023.1:n.708T=
XM_006721516.3:c.601T= XP_006721579.2:p.Tyr201=
XM_011523829.2:c.601T= XP_011522131.1:p.Tyr201=
XM_011523830.2:c.601T= XP_011522132.1:p.Tyr201=
XM_024450741.1:c.601T= XP_024306509.1:p.Tyr201=
XR_934021.2:n.660T=
XR_934022.2:n.660T=
XR_934023.2:n.660T=
NM_000018.4:c.601T= MANE Select NP_000009.1:p.Tyr201=
NM_001033859.3:c.535T= NP_001029031.1:p.Tyr179=
NM_001270447.2:c.670T= NP_001257376.1:p.Tyr224=
NM_001270448.2:c.373T= NP_001257377.1:p.Tyr125=