Canonical Allele Identifier: CA304620762

Gene: LONP1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5701039C>T , CM000681.2:g.5701039C>T	GRCh38
NC_000019.9:g.5701050C>T , CM000681.1:g.5701050C>T	GRCh37
NC_000019.8:g.5652050C>T	NCBI36
NG_033142.1:g.24414G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360614.8:c.1368-112G>A MANE Select	ENSP00000353826.2:n.1368-112G>A
ENST00000360614.7:c.1368-112G>A	ENSP00000353826.2:n.1368-112G>A
ENST00000540670.6:c.780-112G>A	ENSP00000441523.1:n.780-112G>A
ENST00000585374.5:c.1026-112G>A	ENSP00000465585.1:n.1026-112G>A
ENST00000587365.1:c.612-112G>A	ENSP00000468114.1:n.612-112G>A
ENST00000587552.5:n.808-112G>A
ENST00000588589.5:n.642-112G>A
ENST00000590206.1:c.337-112G>A
ENST00000590558.5:c.1175-112G>A	ENSP00000467808.1:n.1175-112G>A
ENST00000590729.5:c.978-112G>A	ENSP00000465139.1:n.978-112G>A
ENST00000593119.5:c.1176-112G>A	ENSP00000468541.1:n.1176-112G>A
NM_001276479.1:c.1176-112G>A	NP_001263408.1:n.1176-112G>A
NM_001276480.1:c.780-112G>A	NP_001263409.1:n.780-112G>A
NM_004793.3:c.1368-112G>A	NP_004784.2:n.1368-112G>A
NR_076392.1:n.1192-112G>A
XM_011528441.3:c.*8-112G>A	XP_011526743.1:n.*8-112G>A
NM_001276479.2:c.1176-112G>A	NP_001263408.1:n.1176-112G>A
NM_004793.4:c.1368-112G>A MANE Select	NP_004784.2:n.1368-112G>A
NR_076392.2:n.1173-112G>A