Canonical Allele Identifier: CA497694022
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7125335A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222016A>G , CM000679.2:g.7222016A>G GRCh38
NC_000017.10:g.7125335A>G , CM000679.1:g.7125335A>G GRCh37
NC_000017.9:g.7066059A>G NCBI36
NG_007975.1:g.7183A>G
NG_008391.2:g.3035T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.687A>G MANE Select ENSP00000349297.5:p.Arg229=
ENST00000322910.9:c.*642A>G ENSP00000325395.5:n.*642A>G
ENST00000350303.9:c.621A>G ENSP00000344152.5:p.Arg207=
ENST00000356839.9:c.687A>G ENSP00000349297.5:p.Arg229=
ENST00000543245.6:c.756A>G ENSP00000438689.2:p.Arg252=
ENST00000577191.5:n.764A>G
ENST00000577857.5:n.503A>G
ENST00000579286.5:n.868A>G
ENST00000580365.1:n.418A>G
ENST00000581378.5:c.405A>G
ENST00000582379.1:n.71A>G
ENST00000583760.1:n.469A>G
NM_000018.3:c.687A>G NP_000009.1:p.Arg229=
NM_001033859.2:c.621A>G NP_001029031.1:p.Arg207=
NM_001270447.1:c.756A>G NP_001257376.1:p.Arg252=
NM_001270448.1:c.459A>G NP_001257377.1:p.Arg153=
XM_006721516.2:c.687A>G XP_006721579.2:p.Arg229=
XM_011523829.1:c.687A>G XP_011522131.1:p.Arg229=
XM_011523830.1:c.687A>G XP_011522132.1:p.Arg229=
XR_934021.1:n.794A>G
XR_934022.1:n.794A>G
XR_934023.1:n.794A>G
XM_006721516.3:c.687A>G XP_006721579.2:p.Arg229=
XM_011523829.2:c.687A>G XP_011522131.1:p.Arg229=
XM_011523830.2:c.687A>G XP_011522132.1:p.Arg229=
XM_024450741.1:c.687A>G XP_024306509.1:p.Arg229=
XR_934021.2:n.746A>G
XR_934022.2:n.746A>G
XR_934023.2:n.746A>G
NM_000018.4:c.687A>G MANE Select NP_000009.1:p.Arg229=
NM_001033859.3:c.621A>G NP_001029031.1:p.Arg207=
NM_001270447.2:c.756A>G NP_001257376.1:p.Arg252=
NM_001270448.2:c.459A>G NP_001257377.1:p.Arg153=
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