Canonical Allele Identifier: CA9114109

Gene: LONP1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5693627G>A , CM000681.2:g.5693627G>A	GRCh38
NC_000019.9:g.5693638G>A , CM000681.1:g.5693638G>A	GRCh37
NC_000019.8:g.5644638G>A	NCBI36
NG_017015.1:g.8367G>A
NG_033142.1:g.31826C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360614.8:c.2463C>T MANE Select	ENSP00000353826.2:p.Ala821=
ENST00000360614.7:c.2463C>T	ENSP00000353826.2:p.Ala821=
ENST00000540670.6:c.1875C>T	ENSP00000441523.1:p.Ala625=
ENST00000585374.5:c.2121C>T	ENSP00000465585.1:p.Ala707=
ENST00000587552.5:n.2201C>T
ENST00000589473.1:c.303C>T	ENSP00000468379.1:p.Ala101=
ENST00000590558.5:c.2270C>T	ENSP00000467808.1:n.2270C>T
ENST00000590729.5:c.2073C>T	ENSP00000465139.1:p.Ala691=
ENST00000593119.5:c.2271C>T	ENSP00000468541.1:p.Ala757=
NM_001276479.1:c.2271C>T	NP_001263408.1:p.Ala757=
NM_001276480.1:c.1875C>T	NP_001263409.1:p.Ala625=
NM_004793.3:c.2463C>T	NP_004784.2:p.Ala821=
NR_076392.1:n.2287C>T
NM_001276479.2:c.2271C>T	NP_001263408.1:p.Ala757=
NM_004793.4:c.2463C>T MANE Select	NP_004784.2:p.Ala821=
NR_076392.2:n.2268C>T