Canonical Allele Identifier: CA403590073

Gene: CLPP

Linked Data - Expert Curation

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6366256A>T , CM000681.2:g.6366256A>T	GRCh38
NC_000019.9:g.6366267A>T , CM000681.1:g.6366267A>T	GRCh37
NC_000019.8:g.6317267A>T	NCBI36
NG_033887.1:g.9805A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245816.11:c.556-2A>T MANE Select	ENSP00000245816.3:n.556-2A>T
ENST00000596605.2:c.151-2A>T
ENST00000597326.6:c.367-2A>T
ENST00000646643.1:c.72+1617A>T	ENSP00000494298.1:n.72+1617A>T
ENST00000245816.8:c.556-2A>T	ENSP00000245816.3:n.556-2A>T
ENST00000596070.1:n.1071-2A>T
ENST00000596149.5:c.295-2A>T	ENSP00000472227.1:n.295-2A>T
ENST00000596605.1:c.107-2A>T	ENSP00000469124.1:n.107-2A>T
ENST00000597326.5:c.367-2A>T	ENSP00000470098.1:n.367-2A>T
NM_006012.2:c.556-2A>T	NP_006003.1:n.556-2A>T
NM_006012.3:c.556-2A>T	NP_006003.1:n.556-2A>T
NM_006012.4:c.556-2A>T MANE Select	NP_006003.1:n.556-2A>T