Canonical Allele Identifier: CA9114975

Gene: LONP1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5711874G>A , CM000681.2:g.5711874G>A	GRCh38
NC_000019.9:g.5711885G>A , CM000681.1:g.5711885G>A	GRCh37
NC_000019.8:g.5662885G>A	NCBI36
NG_033142.1:g.13579C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360614.8:c.767C>T MANE Select	ENSP00000353826.2:p.Ala256Val
ENST00000360614.7:c.767C>T	ENSP00000353826.2:p.Ala256Val
ENST00000540670.6:c.179C>T	ENSP00000441523.1:p.Ala60Val
ENST00000585374.5:c.425C>T	ENSP00000465585.1:p.Ala142Val
ENST00000586617.1:c.*16C>T	ENSP00000468385.1:n.*16C>T
ENST00000587365.1:c.435+589C>T	ENSP00000468114.1:n.435+589C>T
ENST00000587552.5:n.310+1260C>T
ENST00000590558.5:c.574C>T	ENSP00000467808.1:n.574C>T
ENST00000590729.5:c.425C>T	ENSP00000465139.1:p.Ala142Val
ENST00000593119.5:c.575C>T	ENSP00000468541.1:p.Ala192Val
NM_001276479.1:c.575C>T	NP_001263408.1:p.Ala192Val
NM_001276480.1:c.179C>T	NP_001263409.1:p.Ala60Val
NM_004793.3:c.767C>T	NP_004784.2:p.Ala256Val
NR_076392.1:n.591C>T
XM_011528441.1:c.767C>T	XP_011526743.1:p.Ala256Val
XM_011528441.3:c.767C>T	XP_011526743.1:p.Ala256Val
NM_001276479.2:c.575C>T	NP_001263408.1:p.Ala192Val
NM_004793.4:c.767C>T MANE Select	NP_004784.2:p.Ala256Val
NR_076392.2:n.572C>T