Canonical Allele Identifier: CA1969248920

Gene: CSTPP1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47154454C>G , CM000673.2:g.47154454C>G	GRCh38
NC_000011.9:g.47176005C>G , CM000673.1:g.47176005C>G	GRCh37
NC_000011.8:g.47132581C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278460.12:c.366-722C>G MANE Select	ENSP00000278460.8:n.366-722C>G
ENST00000278460.11:c.366-722C>G	ENSP00000278460.7:n.366-722C>G
ENST00000378615.7:c.366-722C>G	ENSP00000367878.3:n.366-722C>G
ENST00000378618.6:c.366-722C>G	ENSP00000367881.2:n.366-722C>G
ENST00000395460.6:c.366-722C>G	ENSP00000378844.2:n.366-722C>G
ENST00000525279.5:c.*272-722C>G	ENSP00000432186.1:n.*272-722C>G
ENST00000525895.5:c.*77-722C>G	ENSP00000432535.1:n.*77-722C>G
ENST00000525953.5:n.60C>G
ENST00000526827.1:c.144-722C>G	ENSP00000433707.1:n.144-722C>G
ENST00000527234.5:n.321-722C>G
ENST00000527268.5:n.502-722C>G
ENST00000527667.5:c.*321-722C>G	ENSP00000436097.1:n.*321-722C>G
ENST00000527784.5:c.*85-722C>G	ENSP00000436571.1:n.*85-722C>G
ENST00000528488.5:c.*302-722C>G	ENSP00000436595.1:n.*302-722C>G
ENST00000529980.5:n.35-722C>G
ENST00000534249.5:c.151-702C>G
NM_001003676.2:c.366-722C>G	NP_001003676.1:n.366-722C>G
NM_001003677.2:c.366-722C>G	NP_001003677.1:n.366-722C>G
NM_001003678.2:c.366-722C>G	NP_001003678.1:n.366-722C>G
NM_001278222.1:c.339-722C>G	NP_001265151.1:n.339-722C>G
NM_024113.4:c.366-722C>G	NP_077018.1:n.366-722C>G
NR_103471.1:n.728-722C>G
NR_103472.1:n.352-722C>G
XM_006718315.1:c.366-722C>G	XP_006718378.1:n.366-722C>G
XM_011520364.1:c.339-722C>G	XP_011518666.1:n.339-722C>G
XM_011520365.1:c.366-722C>G	XP_011518667.1:n.366-722C>G
XR_931257.1:n.683G>C
XM_006718315.2:c.366-722C>G	XP_006718378.1:n.366-722C>G
XM_011520364.2:c.339-722C>G	XP_011518666.1:n.339-722C>G
XM_011520365.3:c.366-722C>G	XP_011518667.1:n.366-722C>G
XM_017018276.2:c.366-722C>G	XP_016873765.1:n.366-722C>G
XM_017018277.2:c.114-722C>G	XP_016873766.1:n.114-722C>G
XM_017018278.1:c.75-722C>G	XP_016873767.1:n.75-722C>G
XM_017018279.1:c.75-722C>G	XP_016873768.1:n.75-722C>G
XM_017018280.1:c.75-722C>G	XP_016873769.1:n.75-722C>G
XM_017018281.1:c.75-722C>G	XP_016873770.1:n.75-722C>G
XM_017018282.1:c.75-722C>G	XP_016873771.1:n.75-722C>G
NM_001003677.3:c.366-722C>G	NP_001003677.1:n.366-722C>G
NM_001003678.3:c.366-722C>G	NP_001003678.1:n.366-722C>G
NM_024113.5:c.366-722C>G MANE Select	NP_077018.1:n.366-722C>G
NR_103471.2:n.656-722C>G
NR_103472.2:n.280-722C>G
NM_001003676.3:c.366-722C>G	NP_001003676.1:n.366-722C>G