Canonical Allele Identifier: CA178189953
Gene: CSPP1 HGNC NCBI

Linked Data

dbSNP Id: rs943782714
gnomAD v4: 8-67158469-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.67158469A>G , CM000670.2:g.67158469A>G GRCh38
NC_000008.10:g.68070704A>G , CM000670.1:g.68070704A>G GRCh37
NC_000008.9:g.68233258A>G NCBI36
NG_034100.1:g.99102A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262210.11:c.2330A>G ENSP00000262210.6:p.Glu777Gly
ENST00000521324.3:c.136A>G
ENST00000674993.1:c.2354A>G ENSP00000502454.1:p.Glu785Gly
ENST00000675306.2:c.1988A>G ENSP00000502421.1:p.Glu663Gly
ENST00000675869.1:c.2069A>G ENSP00000502747.1:p.Glu690Gly
ENST00000675955.1:c.2183A>G ENSP00000501676.1:p.Glu728Gly
ENST00000675990.1:n.3593A>G
ENST00000676113.1:c.2222A>G ENSP00000501645.1:p.Glu741Gly
ENST00000676317.1:c.2249A>G ENSP00000502047.1:p.Glu750Gly
ENST00000676471.1:c.1997A>G ENSP00000503711.1:p.Glu666Gly
ENST00000676534.1:n.5190A>G
ENST00000676567.1:c.*888A>G ENSP00000503427.1:n.*888A>G
ENST00000676573.1:c.1565A>G ENSP00000504532.1:p.Glu522Gly
ENST00000676605.1:c.2372A>G ENSP00000503605.1:p.Glu791Gly
ENST00000676695.1:c.2190A>G ENSP00000503292.1:n.2190A>G
ENST00000676697.1:n.3125A>G
ENST00000676804.1:c.567A>G
ENST00000676847.1:c.2243A>G ENSP00000503336.1:p.Glu748Gly
ENST00000676858.1:c.*225A>G ENSP00000502925.1:n.*225A>G
ENST00000676882.1:c.2150A>G ENSP00000504342.1:p.Glu717Gly
ENST00000676968.1:c.136A>G
ENST00000677009.1:c.2249A>G ENSP00000503297.1:p.Glu750Gly
ENST00000677052.1:n.1762A>G
ENST00000677131.1:c.136A>G
ENST00000677256.1:c.*1983A>G ENSP00000504102.1:n.*1983A>G
ENST00000677430.1:c.2183A>G ENSP00000504177.1:p.Glu728Gly
ENST00000677455.1:n.2137A>G
ENST00000677473.1:c.*280A>G ENSP00000503534.1:n.*280A>G
ENST00000677592.1:c.2231A>G ENSP00000504516.1:p.Glu744Gly
ENST00000677619.1:c.1610A>G ENSP00000504522.1:p.Glu537Gly
ENST00000677697.1:n.232A>G
ENST00000677845.1:c.*635A>G ENSP00000503524.1:n.*635A>G
ENST00000677855.1:c.1572A>G ENSP00000504757.1:n.1572A>G
ENST00000677964.1:c.136A>G
ENST00000678017.1:c.1115A>G ENSP00000504394.1:p.Glu372Gly
ENST00000678138.1:n.2427A>G
ENST00000678156.1:n.1904A>G
ENST00000678318.1:c.1799A>G ENSP00000503690.1:p.Glu600Gly
ENST00000678362.1:c.*1041A>G ENSP00000504317.1:n.*1041A>G
ENST00000678542.1:c.2372A>G ENSP00000503878.1:p.Glu791Gly
ENST00000678616.1:c.2264A>G MANE Select ENSP00000504733.1:p.Glu755Gly
ENST00000678635.1:n.759A>G
ENST00000678645.1:c.2141A>G ENSP00000504031.1:p.Glu714Gly
ENST00000678723.1:c.136A>G
ENST00000678747.1:c.1691A>G ENSP00000503390.1:p.Glu564Gly
ENST00000678807.1:n.1299A>G
ENST00000678895.1:c.136A>G
ENST00000679042.1:n.3089A>G
ENST00000679112.1:c.*2163A>G ENSP00000503739.1:n.*2163A>G
ENST00000679226.1:c.1988A>G ENSP00000503601.1:p.Glu663Gly
ENST00000679274.1:n.1188A>G
ENST00000679295.1:n.1235A>G
ENST00000262210.9:c.2249A>G ENSP00000262210.5:p.Glu750Gly
ENST00000519163.6:c.*2515A>G ENSP00000428694.1:n.*2515A>G
ENST00000519668.1:c.1214A>G ENSP00000430092.1:p.Glu405Gly
ENST00000521168.5:n.254A>G
NM_001291339.1:c.1214A>G NP_001278268.1:p.Glu405Gly
NM_024790.6:c.2249A>G NP_079066.5:p.Glu750Gly
XM_005251305.3:c.2492A>G XP_005251362.2:p.Glu831Gly
XM_006716474.2:c.2339A>G XP_006716537.2:p.Glu780Gly
XM_006716477.2:c.1961A>G XP_006716540.2:p.Glu654Gly
XM_011517598.1:c.2534A>G XP_011515900.1:p.Glu845Gly
XM_011517599.1:c.2510A>G XP_011515901.1:p.Glu837Gly
XM_011517600.1:c.2468A>G XP_011515902.1:p.Glu823Gly
XM_011517601.1:c.2429A>G XP_011515903.1:p.Glu810Gly
XM_011517602.1:c.2387A>G XP_011515904.1:p.Glu796Gly
XM_011517603.1:c.2288A>G XP_011515905.1:p.Glu763Gly
XM_011517604.1:c.2288A>G XP_011515906.1:p.Glu763Gly
XM_011517605.1:c.2288A>G XP_011515907.1:p.Glu763Gly
XM_011517606.1:c.2264A>G XP_011515908.1:p.Glu755Gly
XM_011517607.1:c.2264A>G XP_011515909.1:p.Glu755Gly
XM_011517608.1:c.2183A>G XP_011515910.1:p.Glu728Gly
XM_011517609.1:c.1409A>G XP_011515911.1:p.Glu470Gly
XM_011517610.1:c.929A>G XP_011515912.1:p.Glu310Gly
XM_011517611.1:c.569A>G XP_011515913.1:p.Glu190Gly
NM_001363131.1:c.2183A>G NP_001350060.1:p.Glu728Gly
NM_001363132.1:c.2069A>G NP_001350061.1:p.Glu690Gly
NM_001363133.1:c.1988A>G NP_001350062.1:p.Glu663Gly
NM_001364869.1:c.2330A>G NP_001351798.1:p.Glu777Gly
NM_001364870.1:c.2150A>G NP_001351799.1:p.Glu717Gly
XM_005251305.4:c.2492A>G XP_005251362.2:p.Glu831Gly
XM_006716474.3:c.2339A>G XP_006716537.2:p.Glu780Gly
XM_006716477.3:c.1961A>G XP_006716540.2:p.Glu654Gly
XM_011517598.2:c.2534A>G XP_011515900.1:p.Glu845Gly
XM_011517599.2:c.2510A>G XP_011515901.1:p.Glu837Gly
XM_011517600.2:c.2468A>G XP_011515902.1:p.Glu823Gly
XM_011517601.2:c.2429A>G XP_011515903.1:p.Glu810Gly
XM_011517602.2:c.2387A>G XP_011515904.1:p.Glu796Gly
XM_011517603.2:c.2288A>G XP_011515905.1:p.Glu763Gly
XM_011517607.2:c.2264A>G XP_011515909.1:p.Glu755Gly
XM_011517609.2:c.1409A>G XP_011515911.1:p.Glu470Gly
XM_011517611.3:c.569A>G XP_011515913.1:p.Glu190Gly
XM_017013847.2:c.2393A>G XP_016869336.1:p.Glu798Gly
XM_017013848.2:c.2369A>G XP_016869337.1:p.Glu790Gly
XM_017013849.2:c.2330A>G XP_016869338.1:p.Glu777Gly
XM_017013850.2:c.2288A>G XP_016869339.1:p.Glu763Gly
XM_017013851.2:c.2141A>G XP_016869340.1:p.Glu714Gly
XM_017013852.2:c.2135A>G XP_016869341.1:p.Glu712Gly
XM_017013854.2:c.1937A>G XP_016869343.1:p.Glu646Gly
XM_017013855.2:c.1703A>G XP_016869344.1:p.Glu568Gly
XM_017013856.2:c.1610A>G XP_016869345.1:p.Glu537Gly
XM_017013858.2:c.776A>G XP_016869347.1:p.Glu259Gly
XM_024447278.1:c.2264A>G XP_024303046.1:p.Glu755Gly
XM_024447279.1:c.2183A>G XP_024303047.1:p.Glu728Gly
XM_024447281.1:c.1988A>G XP_024303049.1:p.Glu663Gly
XM_024447282.1:c.1691A>G XP_024303050.1:p.Glu564Gly
XM_024447283.1:c.1367A>G XP_024303051.1:p.Glu456Gly
XM_024447284.1:c.929A>G XP_024303052.1:p.Glu310Gly
NM_001363131.2:c.2183A>G NP_001350060.1:p.Glu728Gly
NM_001363132.2:c.2069A>G NP_001350061.1:p.Glu690Gly
NM_001363133.2:c.1988A>G NP_001350062.1:p.Glu663Gly
NM_001291339.2:c.1214A>G NP_001278268.1:p.Glu405Gly
NM_001382391.1:c.2264A>G MANE Select NP_001369320.1:p.Glu755Gly