Canonical Allele Identifier: CA397723832
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7125600G>T (hg19) chr17:g.7222281G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222281G>T , CM000679.2:g.7222281G>T GRCh38
NC_000017.10:g.7125600G>T , CM000679.1:g.7125600G>T GRCh37
NC_000017.9:g.7066324G>T NCBI36
NG_007975.1:g.7448G>T
NG_008391.2:g.2770C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.857G>T MANE Select ENSP00000349297.5:p.Arg286Met
ENST00000322910.9:c.*812G>T ENSP00000325395.5:n.*812G>T
ENST00000350303.9:c.791G>T ENSP00000344152.5:p.Arg264Met
ENST00000356839.9:c.857G>T ENSP00000349297.5:p.Arg286Met
ENST00000543245.6:c.926G>T ENSP00000438689.2:p.Arg309Met
ENST00000577191.5:n.1029G>T
ENST00000581378.5:c.575G>T
ENST00000582379.1:n.241G>T
NM_000018.3:c.857G>T NP_000009.1:p.Arg286Met
NM_001033859.2:c.791G>T NP_001029031.1:p.Arg264Met
NM_001270447.1:c.926G>T NP_001257376.1:p.Arg309Met
NM_001270448.1:c.629G>T NP_001257377.1:p.Arg210Met
XM_006721516.2:c.857G>T XP_006721579.2:p.Arg286Met
XM_011523829.1:c.857G>T XP_011522131.1:p.Arg286Met
XM_011523830.1:c.857G>T XP_011522132.1:p.Arg286Met
XR_934021.1:n.964G>T
XR_934022.1:n.964G>T
XR_934023.1:n.964G>T
XM_006721516.3:c.857G>T XP_006721579.2:p.Arg286Met
XM_011523829.2:c.857G>T XP_011522131.1:p.Arg286Met
XM_011523830.2:c.857G>T XP_011522132.1:p.Arg286Met
XM_024450741.1:c.857G>T XP_024306509.1:p.Arg286Met
XR_934021.2:n.916G>T
XR_934022.2:n.916G>T
XR_934023.2:n.916G>T
NM_000018.4:c.857G>T MANE Select NP_000009.1:p.Arg286Met
NM_001033859.3:c.791G>T NP_001029031.1:p.Arg264Met
NM_001270447.2:c.926G>T NP_001257376.1:p.Arg309Met
NM_001270448.2:c.629G>T NP_001257377.1:p.Arg210Met
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