Canonical Allele Identifier: CA403536152

Gene: LONP1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5707778G>T , CM000681.2:g.5707778G>T	GRCh38
NC_000019.9:g.5707789G>T , CM000681.1:g.5707789G>T	GRCh37
NC_000019.8:g.5658789G>T	NCBI36
NG_033142.1:g.17675C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360614.8:c.981C>A MANE Select	ENSP00000353826.2:p.Asn327Lys
ENST00000360614.7:c.981C>A	ENSP00000353826.2:p.Asn327Lys
ENST00000540670.6:c.393C>A	ENSP00000441523.1:p.Asn131Lys
ENST00000585374.5:c.639C>A	ENSP00000465585.1:p.Asn213Lys
ENST00000587365.1:c.436-1831C>A	ENSP00000468114.1:n.436-1831C>A
ENST00000587552.5:n.421C>A
ENST00000588589.5:n.255C>A
ENST00000590206.1:c.34C>A
ENST00000590558.5:c.788C>A	ENSP00000467808.1:n.788C>A
ENST00000590729.5:c.591C>A	ENSP00000465139.1:p.Asn197Lys
ENST00000591321.1:n.666C>A
ENST00000593119.5:c.789C>A	ENSP00000468541.1:p.Asn263Lys
NM_001276479.1:c.789C>A	NP_001263408.1:p.Asn263Lys
NM_001276480.1:c.393C>A	NP_001263409.1:p.Asn131Lys
NM_004793.3:c.981C>A	NP_004784.2:p.Asn327Lys
NR_076392.1:n.805C>A
XM_011528441.1:c.981C>A	XP_011526743.1:p.Asn327Lys
XM_011528441.3:c.981C>A	XP_011526743.1:p.Asn327Lys
NM_001276479.2:c.789C>A	NP_001263408.1:p.Asn263Lys
NM_004793.4:c.981C>A MANE Select	NP_004784.2:p.Asn327Lys
NR_076392.2:n.786C>A