Canonical Allele Identifier: CA397722472
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7220673T>G , CM000679.2:g.7220673T>G GRCh38
NC_000017.10:g.7123992T>G , CM000679.1:g.7123992T>G GRCh37
NC_000017.9:g.7064716T>G NCBI36
NG_007975.1:g.5840T>G
NG_008391.2:g.4378A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.274T>G MANE Select ENSP00000349297.5:p.Ser92Ala
ENST00000322910.9:c.*229T>G ENSP00000325395.5:n.*229T>G
ENST00000350303.9:c.208T>G ENSP00000344152.5:p.Ser70Ala
ENST00000356839.9:c.274T>G ENSP00000349297.5:p.Ser92Ala
ENST00000543245.6:c.343T>G ENSP00000438689.2:p.Ser115Ala
ENST00000577191.5:n.351T>G
ENST00000577433.5:n.482T>G
ENST00000577857.5:n.229-93T>G
ENST00000578269.5:n.721T>G
ENST00000578421.1:n.482T>G
ENST00000579286.5:n.455T>G
ENST00000579886.2:c.201+147T>G ENSP00000463246.1:n.201+147T>G
ENST00000580263.5:n.438T>G
ENST00000581562.5:n.321T>G
ENST00000582056.5:n.364T>G
ENST00000582166.1:n.162T>G
ENST00000582356.5:n.473T>G
ENST00000583312.5:c.274T>G ENSP00000467920.1:p.Ser92Ala
ENST00000584103.5:c.274T>G ENSP00000465353.1:p.Ser92Ala
NM_000018.3:c.274T>G NP_000009.1:p.Ser92Ala
NM_001033859.2:c.208T>G NP_001029031.1:p.Ser70Ala
NM_001270447.1:c.343T>G NP_001257376.1:p.Ser115Ala
NM_001270448.1:c.46T>G NP_001257377.1:p.Ser16Ala
XM_006721516.2:c.274T>G XP_006721579.2:p.Ser92Ala
XM_011523829.1:c.274T>G XP_011522131.1:p.Ser92Ala
XM_011523830.1:c.274T>G XP_011522132.1:p.Ser92Ala
XR_934021.1:n.381T>G
XR_934022.1:n.381T>G
XR_934023.1:n.381T>G
XM_006721516.3:c.274T>G XP_006721579.2:p.Ser92Ala
XM_011523829.2:c.274T>G XP_011522131.1:p.Ser92Ala
XM_011523830.2:c.274T>G XP_011522132.1:p.Ser92Ala
XM_024450741.1:c.274T>G XP_024306509.1:p.Ser92Ala
XR_934021.2:n.333T>G
XR_934022.2:n.333T>G
XR_934023.2:n.333T>G
NM_000018.4:c.274T>G MANE Select NP_000009.1:p.Ser92Ala
NM_001033859.3:c.208T>G NP_001029031.1:p.Ser70Ala
NM_001270447.2:c.343T>G NP_001257376.1:p.Ser115Ala
NM_001270448.2:c.46T>G NP_001257377.1:p.Ser16Ala