Canonical Allele Identifier: CA397722463
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7220668A>T , CM000679.2:g.7220668A>T GRCh38
NC_000017.10:g.7123987A>T , CM000679.1:g.7123987A>T GRCh37
NC_000017.9:g.7064711A>T NCBI36
NG_007975.1:g.5835A>T
NG_008391.2:g.4383T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.269A>T MANE Select ENSP00000349297.5:p.Tyr90Phe
ENST00000322910.9:c.*224A>T ENSP00000325395.5:n.*224A>T
ENST00000350303.9:c.203A>T ENSP00000344152.5:p.Tyr68Phe
ENST00000356839.9:c.269A>T ENSP00000349297.5:p.Tyr90Phe
ENST00000543245.6:c.338A>T ENSP00000438689.2:p.Tyr113Phe
ENST00000577191.5:n.346A>T
ENST00000577433.5:n.477A>T
ENST00000577857.5:n.229-98A>T
ENST00000578269.5:n.716A>T
ENST00000578421.1:n.477A>T
ENST00000579286.5:n.450A>T
ENST00000579886.2:c.201+142A>T ENSP00000463246.1:n.201+142A>T
ENST00000580263.5:n.433A>T
ENST00000581562.5:n.316A>T
ENST00000582056.5:n.359A>T
ENST00000582166.1:n.157A>T
ENST00000582356.5:n.468A>T
ENST00000583312.5:c.269A>T ENSP00000467920.1:p.Tyr90Phe
ENST00000584103.5:c.269A>T ENSP00000465353.1:p.Tyr90Phe
NM_000018.3:c.269A>T NP_000009.1:p.Tyr90Phe
NM_001033859.2:c.203A>T NP_001029031.1:p.Tyr68Phe
NM_001270447.1:c.338A>T NP_001257376.1:p.Tyr113Phe
NM_001270448.1:c.41A>T NP_001257377.1:p.Tyr14Phe
XM_006721516.2:c.269A>T XP_006721579.2:p.Tyr90Phe
XM_011523829.1:c.269A>T XP_011522131.1:p.Tyr90Phe
XM_011523830.1:c.269A>T XP_011522132.1:p.Tyr90Phe
XR_934021.1:n.376A>T
XR_934022.1:n.376A>T
XR_934023.1:n.376A>T
XM_006721516.3:c.269A>T XP_006721579.2:p.Tyr90Phe
XM_011523829.2:c.269A>T XP_011522131.1:p.Tyr90Phe
XM_011523830.2:c.269A>T XP_011522132.1:p.Tyr90Phe
XM_024450741.1:c.269A>T XP_024306509.1:p.Tyr90Phe
XR_934021.2:n.328A>T
XR_934022.2:n.328A>T
XR_934023.2:n.328A>T
NM_000018.4:c.269A>T MANE Select NP_000009.1:p.Tyr90Phe
NM_001033859.3:c.203A>T NP_001029031.1:p.Tyr68Phe
NM_001270447.2:c.338A>T NP_001257376.1:p.Tyr113Phe
NM_001270448.2:c.41A>T NP_001257377.1:p.Tyr14Phe