Canonical Allele Identifier: CA497694391
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7127640G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224321G>C , CM000679.2:g.7224321G>C GRCh38
NC_000017.10:g.7127640G>C , CM000679.1:g.7127640G>C GRCh37
NC_000017.9:g.7068364G>C NCBI36
NG_007975.1:g.9488G>C
NG_008391.2:g.730C>G
NG_033038.1:g.15224C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1533G>C MANE Select ENSP00000349297.5:p.Arg511=
ENST00000322910.9:c.*1488G>C ENSP00000325395.5:n.*1488G>C
ENST00000350303.9:c.1467G>C ENSP00000344152.5:p.Arg489=
ENST00000356839.9:c.1533G>C ENSP00000349297.5:p.Arg511=
ENST00000542255.6:c.391G>C
ENST00000543245.6:c.1602G>C ENSP00000438689.2:p.Arg534=
ENST00000578319.5:n.28G>C
ENST00000578711.1:n.817G>C
ENST00000578809.5:n.105G>C
ENST00000579391.1:n.141G>C
ENST00000579425.5:n.649G>C
ENST00000579546.1:c.272G>C
ENST00000579894.5:n.320G>C
ENST00000582450.1:n.41G>C
ENST00000583074.5:n.154G>C
ENST00000583850.5:n.308G>C
ENST00000583858.5:c.464G>C
ENST00000585203.6:n.724G>C
NM_000018.3:c.1533G>C NP_000009.1:p.Arg511=
NM_001033859.2:c.1467G>C NP_001029031.1:p.Arg489=
NM_001270447.1:c.1602G>C NP_001257376.1:p.Arg534=
NM_001270448.1:c.1305G>C NP_001257377.1:p.Arg435=
XM_006721516.2:c.1533G>C XP_006721579.2:p.Arg511=
XM_011523829.1:c.1435G>C XP_011522131.1:p.Ala479Pro
XM_011523830.1:c.1435G>C XP_011522132.1:p.Ala479Pro
XR_934021.1:n.1640G>C
XR_934022.1:n.1542G>C
XR_934023.1:n.1542G>C
XM_006721516.3:c.1533G>C XP_006721579.2:p.Arg511=
XM_011523829.2:c.1435G>C XP_011522131.1:p.Ala479Pro
XM_011523830.2:c.1435G>C XP_011522132.1:p.Ala479Pro
XM_024450741.1:c.1435G>C XP_024306509.1:p.Ala479Pro
XR_934021.2:n.1592G>C
XR_934022.2:n.1494G>C
XR_934023.2:n.1494G>C
NM_000018.4:c.1533G>C MANE Select NP_000009.1:p.Arg511=
NM_001033859.3:c.1467G>C NP_001029031.1:p.Arg489=
NM_001270447.2:c.1602G>C NP_001257376.1:p.Arg534=
NM_001270448.2:c.1305G>C NP_001257377.1:p.Arg435=
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