Canonical Allele Identifier: CA403529639

Gene: LONP1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5696699T>G , CM000681.2:g.5696699T>G	GRCh38
NC_000019.9:g.5696710T>G , CM000681.1:g.5696710T>G	GRCh37
NC_000019.8:g.5647710T>G	NCBI36
NG_033142.1:g.28754A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360614.8:c.1744A>C MANE Select	ENSP00000353826.2:p.Thr582Pro
ENST00000360614.7:c.1744A>C	ENSP00000353826.2:p.Thr582Pro
ENST00000540670.6:c.1156A>C	ENSP00000441523.1:p.Thr386Pro
ENST00000585374.5:c.1402A>C	ENSP00000465585.1:p.Thr468Pro
ENST00000587552.5:n.1184A>C
ENST00000590206.1:c.713A>C
ENST00000590558.5:c.1551A>C	ENSP00000467808.1:n.1551A>C
ENST00000590729.5:c.1354A>C	ENSP00000465139.1:p.Thr452Pro
ENST00000593119.5:c.1552A>C	ENSP00000468541.1:p.Thr518Pro
NM_001276479.1:c.1552A>C	NP_001263408.1:p.Thr518Pro
NM_001276480.1:c.1156A>C	NP_001263409.1:p.Thr386Pro
NM_004793.3:c.1744A>C	NP_004784.2:p.Thr582Pro
NR_076392.1:n.1568A>C
NM_001276479.2:c.1552A>C	NP_001263408.1:p.Thr518Pro
NM_004793.4:c.1744A>C MANE Select	NP_004784.2:p.Thr582Pro
NR_076392.2:n.1549A>C