Canonical Allele Identifier: CA371203863

Gene: CSPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.67132075C>T , CM000670.2:g.67132075C>T	GRCh38
NC_000008.10:g.68044310C>T , CM000670.1:g.68044310C>T	GRCh37
NC_000008.9:g.68206864C>T	NCBI36
NG_034100.1:g.72708C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001382391.1:c.1822C>T MANE Select	NP_001369320.1:p.Gln608Ter
ENST00000678616.1:c.1822C>T MANE Select	ENSP00000504733.1:p.Gln608Ter
NM_001291339.1:c.925C>T	NP_001278268.1:p.Gln309Ter
NM_001291339.2:c.925C>T	NP_001278268.1:p.Gln309Ter
NM_001363131.1:c.1741C>T	NP_001350060.1:p.Gln581Ter
NM_001363131.2:c.1741C>T	NP_001350060.1:p.Gln581Ter
NM_001363132.1:c.1780C>T	NP_001350061.1:p.Gln594Ter
NM_001363132.2:c.1780C>T	NP_001350061.1:p.Gln594Ter
NM_001363133.1:c.1699C>T	NP_001350062.1:p.Gln567Ter
NM_001363133.2:c.1699C>T	NP_001350062.1:p.Gln567Ter
NM_001364869.1:c.1888C>T	NP_001351798.1:p.Gln630Ter
NM_001364870.1:c.1708C>T	NP_001351799.1:p.Gln570Ter
NM_024790.6:c.1807C>T	NP_079066.5:p.Gln603Ter
ENST00000262210.11:c.1888C>T	ENSP00000262210.6:p.Gln630Ter
ENST00000262210.9:c.1807C>T	ENSP00000262210.5:p.Gln603Ter
ENST00000519163.6:c.*2073C>T	ENSP00000428694.1:n.*2073C>T
ENST00000519668.1:c.925C>T	ENSP00000430092.1:p.Gln309Ter
ENST00000674993.1:c.1912C>T	ENSP00000502454.1:p.Gln638Ter
ENST00000675306.2:c.1699C>T	ENSP00000502421.1:p.Gln567Ter
ENST00000675820.1:c.*1613C>T	ENSP00000501959.1:n.*1613C>T
ENST00000675869.1:c.1780C>T	ENSP00000502747.1:p.Gln594Ter
ENST00000675955.1:c.1741C>T	ENSP00000501676.1:p.Gln581Ter
ENST00000676113.1:c.1780C>T	ENSP00000501645.1:p.Gln594Ter
ENST00000676317.1:c.1807C>T	ENSP00000502047.1:p.Gln603Ter
ENST00000676471.1:c.1708C>T	ENSP00000503711.1:p.Gln570Ter
ENST00000676534.1:n.4748C>T
ENST00000676567.1:c.*599C>T	ENSP00000503427.1:n.*599C>T
ENST00000676573.1:c.1276C>T	ENSP00000504532.1:p.Gln426Ter
ENST00000676605.1:c.1930C>T	ENSP00000503605.1:p.Gln644Ter
ENST00000676656.1:n.115C>T
ENST00000676695.1:c.1648C>T	ENSP00000503292.1:n.1648C>T
ENST00000676697.1:n.2583C>T
ENST00000676804.1:c.125C>T
ENST00000676847.1:c.1801C>T	ENSP00000503336.1:p.Gln601Ter
ENST00000676858.1:c.1693C>T	ENSP00000502925.1:p.Gln565Ter
ENST00000676882.1:c.1708C>T	ENSP00000504342.1:p.Gln570Ter
ENST00000677009.1:c.1807C>T	ENSP00000503297.1:p.Gln603Ter
ENST00000677052.1:n.1320C>T
ENST00000677070.1:c.1489C>T	ENSP00000503014.1:p.Gln497Ter
ENST00000677256.1:c.*1541C>T	ENSP00000504102.1:n.*1541C>T
ENST00000677430.1:c.1741C>T	ENSP00000504177.1:p.Gln581Ter
ENST00000677455.1:n.1848C>T
ENST00000677473.1:c.1750C>T	ENSP00000503534.1:p.Gln584Ter
ENST00000677592.1:c.1789C>T	ENSP00000504516.1:p.Gln597Ter
ENST00000677619.1:c.1168C>T	ENSP00000504522.1:p.Gln390Ter
ENST00000677836.1:c.1412C>T	ENSP00000504345.1:n.1412C>T
ENST00000677845.1:c.*193C>T	ENSP00000503524.1:n.*193C>T
ENST00000677855.1:c.1396C>T	ENSP00000504757.1:p.Gln466Ter
ENST00000678017.1:c.826C>T	ENSP00000504394.1:p.Gln276Ter
ENST00000678138.1:n.2138C>T
ENST00000678156.1:n.1462C>T
ENST00000678216.1:n.1414C>T
ENST00000678318.1:c.1357C>T	ENSP00000503690.1:p.Gln453Ter
ENST00000678345.1:c.535C>T	ENSP00000503668.1:p.Gln179Ter
ENST00000678362.1:c.*599C>T	ENSP00000504317.1:n.*599C>T
ENST00000678444.1:c.1506C>T	ENSP00000503879.1:n.1506C>T
ENST00000678542.1:c.1930C>T	ENSP00000503878.1:p.Gln644Ter
ENST00000678553.1:c.1750C>T	ENSP00000503747.1:p.Gln584Ter
ENST00000678635.1:n.317C>T
ENST00000678645.1:c.1699C>T	ENSP00000504031.1:p.Gln567Ter
ENST00000678728.1:c.*599C>T	ENSP00000504830.1:n.*599C>T
ENST00000678747.1:c.1249C>T	ENSP00000503390.1:p.Gln417Ter
ENST00000678807.1:n.1005C>T
ENST00000679042.1:n.2647C>T
ENST00000679112.1:c.*1721C>T	ENSP00000503739.1:n.*1721C>T
ENST00000679226.1:c.1699C>T	ENSP00000503601.1:p.Gln567Ter
ENST00000679274.1:n.746C>T
XM_005251305.3:c.2050C>T	XP_005251362.2:p.Gln684Ter
XM_005251305.4:c.2050C>T	XP_005251362.2:p.Gln684Ter
XM_006716474.2:c.2050C>T	XP_006716537.2:p.Gln684Ter
XM_006716474.3:c.2050C>T	XP_006716537.2:p.Gln684Ter
XM_006716477.2:c.1519C>T	XP_006716540.2:p.Gln507Ter
XM_006716477.3:c.1519C>T	XP_006716540.2:p.Gln507Ter
XM_011517598.1:c.2092C>T	XP_011515900.1:p.Gln698Ter
XM_011517598.2:c.2092C>T	XP_011515900.1:p.Gln698Ter
XM_011517599.1:c.2068C>T	XP_011515901.1:p.Gln690Ter
XM_011517599.2:c.2068C>T	XP_011515901.1:p.Gln690Ter
XM_011517600.1:c.2026C>T	XP_011515902.1:p.Gln676Ter
XM_011517600.2:c.2026C>T	XP_011515902.1:p.Gln676Ter
XM_011517601.1:c.1987C>T	XP_011515903.1:p.Gln663Ter
XM_011517601.2:c.1987C>T	XP_011515903.1:p.Gln663Ter
XM_011517602.1:c.1945C>T	XP_011515904.1:p.Gln649Ter
XM_011517602.2:c.1945C>T	XP_011515904.1:p.Gln649Ter
XM_011517603.1:c.1846C>T	XP_011515905.1:p.Gln616Ter
XM_011517603.2:c.1846C>T	XP_011515905.1:p.Gln616Ter
XM_011517604.1:c.1846C>T	XP_011515906.1:p.Gln616Ter
XM_011517605.1:c.1846C>T	XP_011515907.1:p.Gln616Ter
XM_011517606.1:c.1822C>T	XP_011515908.1:p.Gln608Ter
XM_011517607.1:c.1822C>T	XP_011515909.1:p.Gln608Ter
XM_011517607.2:c.1822C>T	XP_011515909.1:p.Gln608Ter
XM_011517608.1:c.1741C>T	XP_011515910.1:p.Gln581Ter
XM_011517609.1:c.967C>T	XP_011515911.1:p.Gln323Ter
XM_011517609.2:c.967C>T	XP_011515911.1:p.Gln323Ter
XM_011517610.1:c.487C>T	XP_011515912.1:p.Gln163Ter
XM_011517611.1:c.127C>T	XP_011515913.1:p.Gln43Ter
XM_011517611.3:c.127C>T	XP_011515913.1:p.Gln43Ter
XM_017013847.2:c.1951C>T	XP_016869336.1:p.Gln651Ter
XM_017013848.2:c.1927C>T	XP_016869337.1:p.Gln643Ter
XM_017013849.2:c.1888C>T	XP_016869338.1:p.Gln630Ter
XM_017013850.2:c.1846C>T	XP_016869339.1:p.Gln616Ter
XM_017013851.2:c.1699C>T	XP_016869340.1:p.Gln567Ter
XM_017013852.2:c.1846C>T	XP_016869341.1:p.Gln616Ter
XM_017013854.2:c.1495C>T	XP_016869343.1:p.Gln499Ter
XM_017013855.2:c.1414C>T	XP_016869344.1:p.Gln472Ter
XM_017013856.2:c.1168C>T	XP_016869345.1:p.Gln390Ter
XM_017013858.2:c.487C>T	XP_016869347.1:p.Gln163Ter
XM_024447278.1:c.1822C>T	XP_024303046.1:p.Gln608Ter
XM_024447279.1:c.1741C>T	XP_024303047.1:p.Gln581Ter
XM_024447281.1:c.1699C>T	XP_024303049.1:p.Gln567Ter
XM_024447282.1:c.1249C>T	XP_024303050.1:p.Gln417Ter
XM_024447283.1:c.925C>T	XP_024303051.1:p.Gln309Ter
XM_024447284.1:c.487C>T	XP_024303052.1:p.Gln163Ter