Canonical Allele Identifier: CA9114394

Gene: LONP1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5696146C>T , CM000681.2:g.5696146C>T	GRCh38
NC_000019.9:g.5696157C>T , CM000681.1:g.5696157C>T	GRCh37
NC_000019.8:g.5647157C>T	NCBI36
NG_033142.1:g.29307G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360614.8:c.1921G>A MANE Select	ENSP00000353826.2:p.Val641Ile
ENST00000360614.7:c.1921G>A	ENSP00000353826.2:p.Val641Ile
ENST00000540670.6:c.1333G>A	ENSP00000441523.1:p.Val445Ile
ENST00000585374.5:c.1579G>A	ENSP00000465585.1:p.Val527Ile
ENST00000587552.5:n.1659G>A
ENST00000590558.5:c.1728G>A	ENSP00000467808.1:n.1728G>A
ENST00000590729.5:c.1531G>A	ENSP00000465139.1:p.Val511Ile
ENST00000593119.5:c.1729G>A	ENSP00000468541.1:p.Val577Ile
NM_001276479.1:c.1729G>A	NP_001263408.1:p.Val577Ile
NM_001276480.1:c.1333G>A	NP_001263409.1:p.Val445Ile
NM_004793.3:c.1921G>A	NP_004784.2:p.Val641Ile
NR_076392.1:n.1745G>A
NM_001276479.2:c.1729G>A	NP_001263408.1:p.Val577Ile
NM_004793.4:c.1921G>A MANE Select	NP_004784.2:p.Val641Ile
NR_076392.2:n.1726G>A