Canonical Allele Identifier: CA397723069
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221572A>G , CM000679.2:g.7221572A>G GRCh38
NC_000017.10:g.7124891A>G , CM000679.1:g.7124891A>G GRCh37
NC_000017.9:g.7065615A>G NCBI36
NG_007975.1:g.6739A>G
NG_008391.2:g.3479T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.512A>G MANE Select ENSP00000349297.5:p.Asp171Gly
ENST00000322910.9:c.*467A>G ENSP00000325395.5:n.*467A>G
ENST00000350303.9:c.446A>G ENSP00000344152.5:p.Asp149Gly
ENST00000356839.9:c.512A>G ENSP00000349297.5:p.Asp171Gly
ENST00000543245.6:c.581A>G ENSP00000438689.2:p.Asp194Gly
ENST00000577191.5:n.589A>G
ENST00000577433.5:n.720A>G
ENST00000577857.5:n.328A>G
ENST00000579286.5:n.693A>G
ENST00000579886.2:c.350A>G ENSP00000463246.1:p.Asp117Gly
ENST00000580365.1:n.243A>G
ENST00000581378.5:c.230A>G
ENST00000581562.5:n.525-380A>G
ENST00000582166.1:n.493A>G
ENST00000583312.5:c.512A>G ENSP00000467920.1:p.Asp171Gly
ENST00000583760.1:n.294A>G
NM_000018.3:c.512A>G NP_000009.1:p.Asp171Gly
NM_001033859.2:c.446A>G NP_001029031.1:p.Asp149Gly
NM_001270447.1:c.581A>G NP_001257376.1:p.Asp194Gly
NM_001270448.1:c.284A>G NP_001257377.1:p.Asp95Gly
XM_006721516.2:c.512A>G XP_006721579.2:p.Asp171Gly
XM_011523829.1:c.512A>G XP_011522131.1:p.Asp171Gly
XM_011523830.1:c.512A>G XP_011522132.1:p.Asp171Gly
XR_934021.1:n.619A>G
XR_934022.1:n.619A>G
XR_934023.1:n.619A>G
XM_006721516.3:c.512A>G XP_006721579.2:p.Asp171Gly
XM_011523829.2:c.512A>G XP_011522131.1:p.Asp171Gly
XM_011523830.2:c.512A>G XP_011522132.1:p.Asp171Gly
XM_024450741.1:c.512A>G XP_024306509.1:p.Asp171Gly
XR_934021.2:n.571A>G
XR_934022.2:n.571A>G
XR_934023.2:n.571A>G
NM_000018.4:c.512A>G MANE Select NP_000009.1:p.Asp171Gly
NM_001033859.3:c.446A>G NP_001029031.1:p.Asp149Gly
NM_001270447.2:c.581A>G NP_001257376.1:p.Asp194Gly
NM_001270448.2:c.284A>G NP_001257377.1:p.Asp95Gly