Canonical Allele Identifier: CA9114390

Gene: LONP1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5696142G>A , CM000681.2:g.5696142G>A	GRCh38
NC_000019.9:g.5696153G>A , CM000681.1:g.5696153G>A	GRCh37
NC_000019.8:g.5647153G>A	NCBI36
NG_033142.1:g.29311C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360614.8:c.1925C>T MANE Select	ENSP00000353826.2:p.Thr642Met
ENST00000360614.7:c.1925C>T	ENSP00000353826.2:p.Thr642Met
ENST00000540670.6:c.1337C>T	ENSP00000441523.1:p.Thr446Met
ENST00000585374.5:c.1583C>T	ENSP00000465585.1:p.Thr528Met
ENST00000587552.5:n.1663C>T
ENST00000590558.5:c.1732C>T	ENSP00000467808.1:n.1732C>T
ENST00000590729.5:c.1535C>T	ENSP00000465139.1:p.Thr512Met
ENST00000593119.5:c.1733C>T	ENSP00000468541.1:p.Thr578Met
NM_001276479.1:c.1733C>T	NP_001263408.1:p.Thr578Met
NM_001276480.1:c.1337C>T	NP_001263409.1:p.Thr446Met
NM_004793.3:c.1925C>T	NP_004784.2:p.Thr642Met
NR_076392.1:n.1749C>T
NM_001276479.2:c.1733C>T	NP_001263408.1:p.Thr578Met
NM_004793.4:c.1925C>T MANE Select	NP_004784.2:p.Thr642Met
NR_076392.2:n.1730C>T