Canonical Allele Identifier: CA9114220

Gene: LONP1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5694504C>T , CM000681.2:g.5694504C>T	GRCh38
NC_000019.9:g.5694515C>T , CM000681.1:g.5694515C>T	GRCh37
NC_000019.8:g.5645515C>T	NCBI36
NG_033142.1:g.30949G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360614.8:c.2203G>A MANE Select	ENSP00000353826.2:p.Val735Met
ENST00000360614.7:c.2203G>A	ENSP00000353826.2:p.Val735Met
ENST00000540670.6:c.1615G>A	ENSP00000441523.1:p.Val539Met
ENST00000585374.5:c.1861G>A	ENSP00000465585.1:p.Val621Met
ENST00000587552.5:n.1941G>A
ENST00000589473.1:c.43G>A	ENSP00000468379.1:p.Val15Met
ENST00000590558.5:c.2010G>A	ENSP00000467808.1:n.2010G>A
ENST00000590729.5:c.1813G>A	ENSP00000465139.1:p.Val605Met
ENST00000593119.5:c.2011G>A	ENSP00000468541.1:p.Val671Met
NM_001276479.1:c.2011G>A	NP_001263408.1:p.Val671Met
NM_001276480.1:c.1615G>A	NP_001263409.1:p.Val539Met
NM_004793.3:c.2203G>A	NP_004784.2:p.Val735Met
NR_076392.1:n.2027G>A
NM_001276479.2:c.2011G>A	NP_001263408.1:p.Val671Met
NM_004793.4:c.2203G>A MANE Select	NP_004784.2:p.Val735Met
NR_076392.2:n.2008G>A