Canonical Allele Identifier: CA143978

Gene: CLPP

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6361944A>G , CM000681.2:g.6361944A>G	GRCh38
NC_000019.9:g.6361955A>G , CM000681.1:g.6361955A>G	GRCh37
NC_000019.8:g.6312955A>G	NCBI36
NG_033887.1:g.5493A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245816.11:c.270+4A>G MANE Select	ENSP00000245816.3:n.270+4A>G
ENST00000596605.2:c.53+4A>G
ENST00000597326.6:c.98+4A>G
ENST00000245816.8:c.270+4A>G	ENSP00000245816.3:n.270+4A>G
ENST00000594780.1:n.171+4A>G
ENST00000596070.1:n.284A>G
ENST00000596149.5:c.9+4A>G	ENSP00000472227.1:n.9+4A>G
ENST00000596605.1:c.9+4A>G	ENSP00000469124.1:n.9+4A>G
ENST00000597326.5:c.98+4A>G	ENSP00000470098.1:n.98+4A>G
NM_006012.2:c.270+4A>G	NP_006003.1:n.270+4A>G
NM_006012.3:c.270+4A>G	NP_006003.1:n.270+4A>G
NM_006012.4:c.270+4A>G MANE Select	NP_006003.1:n.270+4A>G