Canonical Allele Identifier: CA397722827
Gene: ACADVL HGNC NCBI

Linked Data

dbSNP Id: rs759618804

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7220981C>G , CM000679.2:g.7220981C>G GRCh38
NC_000017.10:g.7124300C>G , CM000679.1:g.7124300C>G GRCh37
NC_000017.9:g.7065024C>G NCBI36
NG_007975.1:g.6148C>G
NG_008391.2:g.4070G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.400C>G MANE Select ENSP00000349297.5:p.Gln134Glu
ENST00000322910.9:c.*355C>G ENSP00000325395.5:n.*355C>G
ENST00000350303.9:c.334C>G ENSP00000344152.5:p.Gln112Glu
ENST00000356839.9:c.400C>G ENSP00000349297.5:p.Gln134Glu
ENST00000543245.6:c.469C>G ENSP00000438689.2:p.Gln157Glu
ENST00000577191.5:n.477C>G
ENST00000577433.5:n.608C>G
ENST00000577857.5:n.293+151C>G
ENST00000579286.5:n.581C>G
ENST00000579886.2:c.238C>G ENSP00000463246.1:p.Gln80Glu
ENST00000580365.1:n.131C>G
ENST00000581378.5:c.99C>G
ENST00000581562.5:n.447C>G
ENST00000582056.5:n.583C>G
ENST00000582166.1:n.381C>G
ENST00000583312.5:c.400C>G ENSP00000467920.1:p.Gln134Glu
ENST00000584103.5:c.433C>G ENSP00000465353.1:p.Gln145Glu
NM_000018.3:c.400C>G NP_000009.1:p.Gln134Glu
NM_001033859.2:c.334C>G NP_001029031.1:p.Gln112Glu
NM_001270447.1:c.469C>G NP_001257376.1:p.Gln157Glu
NM_001270448.1:c.172C>G NP_001257377.1:p.Gln58Glu
XM_006721516.2:c.400C>G XP_006721579.2:p.Gln134Glu
XM_011523829.1:c.400C>G XP_011522131.1:p.Gln134Glu
XM_011523830.1:c.400C>G XP_011522132.1:p.Gln134Glu
XR_934021.1:n.507C>G
XR_934022.1:n.507C>G
XR_934023.1:n.507C>G
XM_006721516.3:c.400C>G XP_006721579.2:p.Gln134Glu
XM_011523829.2:c.400C>G XP_011522131.1:p.Gln134Glu
XM_011523830.2:c.400C>G XP_011522132.1:p.Gln134Glu
XM_024450741.1:c.400C>G XP_024306509.1:p.Gln134Glu
XR_934021.2:n.459C>G
XR_934022.2:n.459C>G
XR_934023.2:n.459C>G
NM_000018.4:c.400C>G MANE Select NP_000009.1:p.Gln134Glu
NM_001033859.3:c.334C>G NP_001029031.1:p.Gln112Glu
NM_001270447.2:c.469C>G NP_001257376.1:p.Gln157Glu
NM_001270448.2:c.172C>G NP_001257377.1:p.Gln58Glu