Canonical Allele Identifier: CA497694396
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7127646A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224327A>T , CM000679.2:g.7224327A>T GRCh38
NC_000017.10:g.7127646A>T , CM000679.1:g.7127646A>T GRCh37
NC_000017.9:g.7068370A>T NCBI36
NG_007975.1:g.9494A>T
NG_008391.2:g.724T>A
NG_033038.1:g.15218T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1539A>T MANE Select ENSP00000349297.5:p.Ala513=
ENST00000322910.9:c.*1494A>T ENSP00000325395.5:n.*1494A>T
ENST00000350303.9:c.1473A>T ENSP00000344152.5:p.Ala491=
ENST00000356839.9:c.1539A>T ENSP00000349297.5:p.Ala513=
ENST00000542255.6:c.397A>T
ENST00000543245.6:c.1608A>T ENSP00000438689.2:p.Ala536=
ENST00000578319.5:n.34A>T
ENST00000578711.1:n.823A>T
ENST00000578809.5:n.111A>T
ENST00000579391.1:n.147A>T
ENST00000579425.5:n.655A>T
ENST00000579546.1:c.278A>T
ENST00000579894.5:n.326A>T
ENST00000582450.1:n.47A>T
ENST00000583074.5:n.160A>T
ENST00000583850.5:n.314A>T
ENST00000583858.5:c.470A>T
ENST00000585203.6:n.730A>T
NM_000018.3:c.1539A>T NP_000009.1:p.Ala513=
NM_001033859.2:c.1473A>T NP_001029031.1:p.Ala491=
NM_001270447.1:c.1608A>T NP_001257376.1:p.Ala536=
NM_001270448.1:c.1311A>T NP_001257377.1:p.Ala437=
XM_006721516.2:c.1539A>T XP_006721579.2:p.Ala513=
XM_011523829.1:c.1441A>T XP_011522131.1:p.Arg481Trp
XM_011523830.1:c.1441A>T XP_011522132.1:p.Arg481Trp
XR_934021.1:n.1646A>T
XR_934022.1:n.1548A>T
XR_934023.1:n.1548A>T
XM_006721516.3:c.1539A>T XP_006721579.2:p.Ala513=
XM_011523829.2:c.1441A>T XP_011522131.1:p.Arg481Trp
XM_011523830.2:c.1441A>T XP_011522132.1:p.Arg481Trp
XM_024450741.1:c.1441A>T XP_024306509.1:p.Arg481Trp
XR_934021.2:n.1598A>T
XR_934022.2:n.1500A>T
XR_934023.2:n.1500A>T
NM_000018.4:c.1539A>T MANE Select NP_000009.1:p.Ala513=
NM_001033859.3:c.1473A>T NP_001029031.1:p.Ala491=
NM_001270447.2:c.1608A>T NP_001257376.1:p.Ala536=
NM_001270448.2:c.1311A>T NP_001257377.1:p.Ala437=
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