Canonical Allele Identifier: CA397722997
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221538T>G , CM000679.2:g.7221538T>G GRCh38
NC_000017.10:g.7124857T>G , CM000679.1:g.7124857T>G GRCh37
NC_000017.9:g.7065581T>G NCBI36
NG_007975.1:g.6705T>G
NG_008391.2:g.3513A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000356839.10:c.478T>G MANE Select ENSP00000349297.5:p.Tyr160Asp
ENST00000322910.9:c.*433T>G ENSP00000325395.5:n.*433T>G
ENST00000350303.9:c.412T>G ENSP00000344152.5:p.Tyr138Asp
ENST00000356839.9:c.478T>G ENSP00000349297.5:p.Tyr160Asp
ENST00000543245.6:c.547T>G ENSP00000438689.2:p.Tyr183Asp
ENST00000577191.5:n.555T>G
ENST00000577433.5:n.686T>G
ENST00000577857.5:n.294T>G
ENST00000579286.5:n.659T>G
ENST00000579886.2:c.316T>G ENSP00000463246.1:p.Tyr106Asp
ENST00000580365.1:n.209T>G
ENST00000581378.5:c.196T>G
ENST00000581562.5:n.525-414T>G
ENST00000582166.1:n.459T>G
ENST00000583312.5:c.478T>G ENSP00000467920.1:p.Tyr160Asp
ENST00000583760.1:n.260T>G
NM_000018.3:c.478T>G NP_000009.1:p.Tyr160Asp
NM_001033859.2:c.412T>G NP_001029031.1:p.Tyr138Asp
NM_001270447.1:c.547T>G NP_001257376.1:p.Tyr183Asp
NM_001270448.1:c.250T>G NP_001257377.1:p.Tyr84Asp
XM_006721516.2:c.478T>G XP_006721579.2:p.Tyr160Asp
XM_011523829.1:c.478T>G XP_011522131.1:p.Tyr160Asp
XM_011523830.1:c.478T>G XP_011522132.1:p.Tyr160Asp
XR_934021.1:n.585T>G
XR_934022.1:n.585T>G
XR_934023.1:n.585T>G
XM_006721516.3:c.478T>G XP_006721579.2:p.Tyr160Asp
XM_011523829.2:c.478T>G XP_011522131.1:p.Tyr160Asp
XM_011523830.2:c.478T>G XP_011522132.1:p.Tyr160Asp
XM_024450741.1:c.478T>G XP_024306509.1:p.Tyr160Asp
XR_934021.2:n.537T>G
XR_934022.2:n.537T>G
XR_934023.2:n.537T>G
NM_000018.4:c.478T>G MANE Select NP_000009.1:p.Tyr160Asp
NM_001033859.3:c.412T>G NP_001029031.1:p.Tyr138Asp
NM_001270447.2:c.547T>G NP_001257376.1:p.Tyr183Asp
NM_001270448.2:c.250T>G NP_001257377.1:p.Tyr84Asp