Canonical Allele Identifier: CA403535210

Gene: LONP1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5707076T>C , CM000681.2:g.5707076T>C	GRCh38
NC_000019.9:g.5707087T>C , CM000681.1:g.5707087T>C	GRCh37
NC_000019.8:g.5658087T>C	NCBI36
NG_033142.1:g.18377A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360614.8:c.1130A>G MANE Select	ENSP00000353826.2:p.Gln377Arg
ENST00000360614.7:c.1130A>G	ENSP00000353826.2:p.Gln377Arg
ENST00000540670.6:c.542A>G	ENSP00000441523.1:p.Gln181Arg
ENST00000585374.5:c.788A>G	ENSP00000465585.1:p.Gln263Arg
ENST00000587365.1:c.436-1129A>G	ENSP00000468114.1:n.436-1129A>G
ENST00000587552.5:n.570A>G
ENST00000588589.5:n.404A>G
ENST00000590206.1:c.115+621A>G
ENST00000590558.5:c.937A>G	ENSP00000467808.1:n.937A>G
ENST00000590729.5:c.740A>G	ENSP00000465139.1:p.Gln247Arg
ENST00000591321.1:n.815A>G
ENST00000593119.5:c.938A>G	ENSP00000468541.1:p.Gln313Arg
NM_001276479.1:c.938A>G	NP_001263408.1:p.Gln313Arg
NM_001276480.1:c.542A>G	NP_001263409.1:p.Gln181Arg
NM_004793.3:c.1130A>G	NP_004784.2:p.Gln377Arg
NR_076392.1:n.954A>G
XM_011528441.1:c.1130A>G	XP_011526743.1:p.Gln377Arg
XM_011528441.3:c.1130A>G	XP_011526743.1:p.Gln377Arg
NM_001276479.2:c.938A>G	NP_001263408.1:p.Gln313Arg
NM_004793.4:c.1130A>G MANE Select	NP_004784.2:p.Gln377Arg
NR_076392.2:n.935A>G