Canonical Allele Identifier: CA2245698584
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7220632T= , CM000679.2:g.7220632T= GRCh38
NC_000017.10:g.7123951T= , CM000679.1:g.7123951T= GRCh37
NC_000017.9:g.7064675T= NCBI36
NG_007975.1:g.5799T=
NG_008391.2:g.4419A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.233T= MANE Select ENSP00000349297.5:p.Phe78=
ENST00000322910.9:c.*188T= ENSP00000325395.5:n.*188T=
ENST00000350303.9:c.167T= ENSP00000344152.5:p.Phe56=
ENST00000356839.9:c.233T= ENSP00000349297.5:p.Phe78=
ENST00000543245.6:c.302T= ENSP00000438689.2:p.Phe101=
ENST00000577191.5:n.310T=
ENST00000577433.5:n.441T=
ENST00000577857.5:n.229-134T=
ENST00000578269.5:n.680T=
ENST00000578421.1:n.441T=
ENST00000579286.5:n.414T=
ENST00000579886.2:c.201+106T= ENSP00000463246.1:n.201+106T=
ENST00000580263.5:n.397T=
ENST00000581562.5:n.280T=
ENST00000582056.5:n.323T=
ENST00000582166.1:n.121T=
ENST00000582356.5:n.432T=
ENST00000583312.5:c.233T= ENSP00000467920.1:p.Phe78=
ENST00000584103.5:c.233T= ENSP00000465353.1:p.Phe78=
NM_000018.3:c.233T= NP_000009.1:p.Phe78=
NM_001033859.2:c.167T= NP_001029031.1:p.Phe56=
NM_001270447.1:c.302T= NP_001257376.1:p.Phe101=
NM_001270448.1:c.5T= NP_001257377.1:p.Phe2=
XM_006721516.2:c.233T= XP_006721579.2:p.Phe78=
XM_011523829.1:c.233T= XP_011522131.1:p.Phe78=
XM_011523830.1:c.233T= XP_011522132.1:p.Phe78=
XR_934021.1:n.340T=
XR_934022.1:n.340T=
XR_934023.1:n.340T=
XM_006721516.3:c.233T= XP_006721579.2:p.Phe78=
XM_011523829.2:c.233T= XP_011522131.1:p.Phe78=
XM_011523830.2:c.233T= XP_011522132.1:p.Phe78=
XM_024450741.1:c.233T= XP_024306509.1:p.Phe78=
XR_934021.2:n.292T=
XR_934022.2:n.292T=
XR_934023.2:n.292T=
NM_000018.4:c.233T= MANE Select NP_000009.1:p.Phe78=
NM_001033859.3:c.167T= NP_001029031.1:p.Phe56=
NM_001270447.2:c.302T= NP_001257376.1:p.Phe101=
NM_001270448.2:c.5T= NP_001257377.1:p.Phe2=