Canonical Allele Identifier: CA15701965

Gene: CSTPP1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46986828A>G , CM000673.2:g.46986828A>G	GRCh38
NC_000011.9:g.47008379A>G , CM000673.1:g.47008379A>G	GRCh37
NC_000011.8:g.46964955A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278460.12:c.47-380A>G MANE Select	ENSP00000278460.8:n.47-380A>G
ENST00000278460.11:c.47-380A>G	ENSP00000278460.7:n.47-380A>G
ENST00000378615.7:c.47-380A>G	ENSP00000367878.3:n.47-380A>G
ENST00000378618.6:c.47-380A>G	ENSP00000367881.2:n.47-380A>G
ENST00000395460.6:c.47-380A>G	ENSP00000378844.2:n.47-380A>G
ENST00000522712.6:n.108-380A>G
ENST00000525279.5:c.47-380A>G	ENSP00000432186.1:n.47-380A>G
ENST00000525895.5:c.46+49977A>G	ENSP00000432535.1:n.46+49977A>G
ENST00000526424.5:c.186-380A>G	ENSP00000434380.1:n.186-380A>G
ENST00000527234.5:n.104+49977A>G
ENST00000527667.5:c.47-380A>G	ENSP00000436097.1:n.47-380A>G
ENST00000527784.5:c.47-380A>G	ENSP00000436571.1:n.47-380A>G
ENST00000528488.5:c.47-380A>G	ENSP00000436595.1:n.47-380A>G
ENST00000531648.5:n.105-380A>G
ENST00000532633.5:c.47-380A>G	ENSP00000437259.1:n.47-380A>G
ENST00000532840.5:n.93-380A>G
ENST00000533124.5:n.163+49977A>G
NM_001003676.2:c.47-380A>G	NP_001003676.1:n.47-380A>G
NM_001003677.2:c.47-380A>G	NP_001003677.1:n.47-380A>G
NM_001003678.2:c.47-380A>G	NP_001003678.1:n.47-380A>G
NM_001278222.1:c.122+49977A>G	NP_001265151.1:n.122+49977A>G
NM_024113.4:c.47-380A>G	NP_077018.1:n.47-380A>G
NR_103471.1:n.164-380A>G
NR_103472.1:n.164-380A>G
XM_006718315.1:c.47-380A>G	XP_006718378.1:n.47-380A>G
XM_011520364.1:c.122+49977A>G	XP_011518666.1:n.122+49977A>G
XM_011520365.1:c.47-380A>G	XP_011518667.1:n.47-380A>G
XM_006718315.2:c.47-380A>G	XP_006718378.1:n.47-380A>G
XM_011520364.2:c.122+49977A>G	XP_011518666.1:n.122+49977A>G
XM_011520365.3:c.47-380A>G	XP_011518667.1:n.47-380A>G
XM_017018276.2:c.47-380A>G	XP_016873765.1:n.47-380A>G
XM_017018277.2:c.-75-380A>G	XP_016873766.1:n.-75-380A>G
XM_017018278.1:c.-427-380A>G	XP_016873767.1:n.-427-380A>G
XM_017018279.1:c.-490-380A>G	XP_016873768.1:n.-490-380A>G
XM_017018280.1:c.-1215-380A>G	XP_016873769.1:n.-1215-380A>G
XM_017018281.1:c.-1113+49977A>G	XP_016873770.1:n.-1113+49977A>G
XM_017018282.1:c.-427-380A>G	XP_016873771.1:n.-427-380A>G
NM_001003677.3:c.47-380A>G	NP_001003677.1:n.47-380A>G
NM_001003678.3:c.47-380A>G	NP_001003678.1:n.47-380A>G
NM_024113.5:c.47-380A>G MANE Select	NP_077018.1:n.47-380A>G
NR_103471.2:n.92-380A>G
NR_103472.2:n.92-380A>G
NM_001003676.3:c.47-380A>G	NP_001003676.1:n.47-380A>G