Canonical Allele Identifier: CA403589588

Gene: CLPP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6364517A>G , CM000681.2:g.6364517A>G	GRCh38
NC_000019.9:g.6364528A>G , CM000681.1:g.6364528A>G	GRCh37
NC_000019.8:g.6315528A>G	NCBI36
NG_033887.1:g.8066A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245816.11:c.433A>G MANE Select	ENSP00000245816.3:p.Thr145Ala
ENST00000596605.2:c.151-1741A>G
ENST00000597326.6:c.244A>G
ENST00000245816.8:c.433A>G	ENSP00000245816.3:p.Thr145Ala
ENST00000594780.1:n.334A>G
ENST00000596070.1:n.948A>G
ENST00000596149.5:c.172A>G	ENSP00000472227.1:p.Thr58Ala
ENST00000596605.1:c.107-1741A>G	ENSP00000469124.1:n.107-1741A>G
ENST00000597326.5:c.244A>G	ENSP00000470098.1:p.Thr82Ala
NM_006012.2:c.433A>G	NP_006003.1:p.Thr145Ala
NM_006012.3:c.433A>G	NP_006003.1:p.Thr145Ala
NM_006012.4:c.433A>G MANE Select	NP_006003.1:p.Thr145Ala