Canonical Allele Identifier: CA9114366
Gene: LONP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5696090C>T , CM000681.2:g.5696090C>T GRCh38
NC_000019.9:g.5696101C>T , CM000681.1:g.5696101C>T GRCh37
NC_000019.8:g.5647101C>T NCBI36
NG_033142.1:g.29363G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360614.8:c.1977G>A MANE Select ENSP00000353826.2:p.Ser659=
ENST00000360614.7:c.1977G>A ENSP00000353826.2:p.Ser659=
ENST00000540670.6:c.1389G>A ENSP00000441523.1:p.Ser463=
ENST00000585374.5:c.1635G>A ENSP00000465585.1:p.Ser545=
ENST00000587552.5:n.1715G>A
ENST00000590558.5:c.1784G>A ENSP00000467808.1:n.1784G>A
ENST00000590729.5:c.1587G>A ENSP00000465139.1:p.Ser529=
ENST00000593119.5:c.1785G>A ENSP00000468541.1:p.Ser595=
NM_001276479.1:c.1785G>A NP_001263408.1:p.Ser595=
NM_001276480.1:c.1389G>A NP_001263409.1:p.Ser463=
NM_004793.3:c.1977G>A NP_004784.2:p.Ser659=
NR_076392.1:n.1801G>A
NM_001276479.2:c.1785G>A NP_001263408.1:p.Ser595=
NM_004793.4:c.1977G>A MANE Select NP_004784.2:p.Ser659=
NR_076392.2:n.1782G>A