Canonical Allele Identifier: CA403528909

Gene: LONP1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5696158A>C , CM000681.2:g.5696158A>C	GRCh38
NC_000019.9:g.5696169A>C , CM000681.1:g.5696169A>C	GRCh37
NC_000019.8:g.5647169A>C	NCBI36
NG_033142.1:g.29295T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360614.8:c.1909T>G MANE Select	ENSP00000353826.2:p.Cys637Gly
ENST00000360614.7:c.1909T>G	ENSP00000353826.2:p.Cys637Gly
ENST00000540670.6:c.1321T>G	ENSP00000441523.1:p.Cys441Gly
ENST00000585374.5:c.1567T>G	ENSP00000465585.1:p.Cys523Gly
ENST00000587552.5:n.1647T>G
ENST00000590558.5:c.1716T>G	ENSP00000467808.1:n.1716T>G
ENST00000590729.5:c.1519T>G	ENSP00000465139.1:p.Cys507Gly
ENST00000593119.5:c.1717T>G	ENSP00000468541.1:p.Cys573Gly
NM_001276479.1:c.1717T>G	NP_001263408.1:p.Cys573Gly
NM_001276480.1:c.1321T>G	NP_001263409.1:p.Cys441Gly
NM_004793.3:c.1909T>G	NP_004784.2:p.Cys637Gly
NR_076392.1:n.1733T>G
NM_001276479.2:c.1717T>G	NP_001263408.1:p.Cys573Gly
NM_004793.4:c.1909T>G MANE Select	NP_004784.2:p.Cys637Gly
NR_076392.2:n.1714T>G