Canonical Allele Identifier: CA371188384

Gene: CSPP1

Linked Data

• MyVariant Identifiers: chr8:g.68070700A>T (hg19) ; chr8:g.67158465A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.67158465A>T , CM000670.2:g.67158465A>T	GRCh38
NC_000008.10:g.68070700A>T , CM000670.1:g.68070700A>T	GRCh37
NC_000008.9:g.68233254A>T	NCBI36
NG_034100.1:g.99098A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262210.11:c.2326A>T	ENSP00000262210.6:p.Arg776Ter
ENST00000521324.3:c.132A>T
ENST00000674993.1:c.2350A>T	ENSP00000502454.1:p.Arg784Ter
ENST00000675306.2:c.1984A>T	ENSP00000502421.1:p.Arg662Ter
ENST00000675869.1:c.2065A>T	ENSP00000502747.1:p.Arg689Ter
ENST00000675955.1:c.2179A>T	ENSP00000501676.1:p.Arg727Ter
ENST00000675990.1:n.3589A>T
ENST00000676113.1:c.2218A>T	ENSP00000501645.1:p.Arg740Ter
ENST00000676317.1:c.2245A>T	ENSP00000502047.1:p.Arg749Ter
ENST00000676471.1:c.1993A>T	ENSP00000503711.1:p.Arg665Ter
ENST00000676534.1:n.5186A>T
ENST00000676567.1:c.*884A>T	ENSP00000503427.1:n.*884A>T
ENST00000676573.1:c.1561A>T	ENSP00000504532.1:p.Arg521Ter
ENST00000676605.1:c.2368A>T	ENSP00000503605.1:p.Arg790Ter
ENST00000676695.1:c.2186A>T	ENSP00000503292.1:n.2186A>T
ENST00000676697.1:n.3121A>T
ENST00000676804.1:c.563A>T
ENST00000676847.1:c.2239A>T	ENSP00000503336.1:p.Arg747Ter
ENST00000676858.1:c.*221A>T	ENSP00000502925.1:n.*221A>T
ENST00000676882.1:c.2146A>T	ENSP00000504342.1:p.Arg716Ter
ENST00000676968.1:c.132A>T
ENST00000677009.1:c.2245A>T	ENSP00000503297.1:p.Arg749Ter
ENST00000677052.1:n.1758A>T
ENST00000677131.1:c.132A>T
ENST00000677256.1:c.*1979A>T	ENSP00000504102.1:n.*1979A>T
ENST00000677430.1:c.2179A>T	ENSP00000504177.1:p.Arg727Ter
ENST00000677455.1:n.2133A>T
ENST00000677473.1:c.*276A>T	ENSP00000503534.1:n.*276A>T
ENST00000677592.1:c.2227A>T	ENSP00000504516.1:p.Arg743Ter
ENST00000677619.1:c.1606A>T	ENSP00000504522.1:p.Arg536Ter
ENST00000677697.1:n.228A>T
ENST00000677845.1:c.*631A>T	ENSP00000503524.1:n.*631A>T
ENST00000677855.1:c.1568A>T	ENSP00000504757.1:n.1568A>T
ENST00000677964.1:c.132A>T
ENST00000678017.1:c.1111A>T	ENSP00000504394.1:p.Arg371Ter
ENST00000678138.1:n.2423A>T
ENST00000678156.1:n.1900A>T
ENST00000678318.1:c.1795A>T	ENSP00000503690.1:p.Arg599Ter
ENST00000678362.1:c.*1037A>T	ENSP00000504317.1:n.*1037A>T
ENST00000678542.1:c.2368A>T	ENSP00000503878.1:p.Arg790Ter
ENST00000678616.1:c.2260A>T MANE Select	ENSP00000504733.1:p.Arg754Ter
ENST00000678635.1:n.755A>T
ENST00000678645.1:c.2137A>T	ENSP00000504031.1:p.Arg713Ter
ENST00000678723.1:c.132A>T
ENST00000678747.1:c.1687A>T	ENSP00000503390.1:p.Arg563Ter
ENST00000678807.1:n.1295A>T
ENST00000678895.1:c.132A>T
ENST00000679042.1:n.3085A>T
ENST00000679112.1:c.*2159A>T	ENSP00000503739.1:n.*2159A>T
ENST00000679226.1:c.1984A>T	ENSP00000503601.1:p.Arg662Ter
ENST00000679274.1:n.1184A>T
ENST00000679295.1:n.1231A>T
ENST00000262210.9:c.2245A>T	ENSP00000262210.5:p.Arg749Ter
ENST00000519163.6:c.*2511A>T	ENSP00000428694.1:n.*2511A>T
ENST00000519668.1:c.1210A>T	ENSP00000430092.1:p.Arg404Ter
ENST00000521168.5:n.250A>T
NM_001291339.1:c.1210A>T	NP_001278268.1:p.Arg404Ter
NM_024790.6:c.2245A>T	NP_079066.5:p.Arg749Ter
XM_005251305.3:c.2488A>T	XP_005251362.2:p.Arg830Ter
XM_006716474.2:c.2335A>T	XP_006716537.2:p.Arg779Ter
XM_006716477.2:c.1957A>T	XP_006716540.2:p.Arg653Ter
XM_011517598.1:c.2530A>T	XP_011515900.1:p.Arg844Ter
XM_011517599.1:c.2506A>T	XP_011515901.1:p.Arg836Ter
XM_011517600.1:c.2464A>T	XP_011515902.1:p.Arg822Ter
XM_011517601.1:c.2425A>T	XP_011515903.1:p.Arg809Ter
XM_011517602.1:c.2383A>T	XP_011515904.1:p.Arg795Ter
XM_011517603.1:c.2284A>T	XP_011515905.1:p.Arg762Ter
XM_011517604.1:c.2284A>T	XP_011515906.1:p.Arg762Ter
XM_011517605.1:c.2284A>T	XP_011515907.1:p.Arg762Ter
XM_011517606.1:c.2260A>T	XP_011515908.1:p.Arg754Ter
XM_011517607.1:c.2260A>T	XP_011515909.1:p.Arg754Ter
XM_011517608.1:c.2179A>T	XP_011515910.1:p.Arg727Ter
XM_011517609.1:c.1405A>T	XP_011515911.1:p.Arg469Ter
XM_011517610.1:c.925A>T	XP_011515912.1:p.Arg309Ter
XM_011517611.1:c.565A>T	XP_011515913.1:p.Arg189Ter
NM_001363131.1:c.2179A>T	NP_001350060.1:p.Arg727Ter
NM_001363132.1:c.2065A>T	NP_001350061.1:p.Arg689Ter
NM_001363133.1:c.1984A>T	NP_001350062.1:p.Arg662Ter
NM_001364869.1:c.2326A>T	NP_001351798.1:p.Arg776Ter
NM_001364870.1:c.2146A>T	NP_001351799.1:p.Arg716Ter
XM_005251305.4:c.2488A>T	XP_005251362.2:p.Arg830Ter
XM_006716474.3:c.2335A>T	XP_006716537.2:p.Arg779Ter
XM_006716477.3:c.1957A>T	XP_006716540.2:p.Arg653Ter
XM_011517598.2:c.2530A>T	XP_011515900.1:p.Arg844Ter
XM_011517599.2:c.2506A>T	XP_011515901.1:p.Arg836Ter
XM_011517600.2:c.2464A>T	XP_011515902.1:p.Arg822Ter
XM_011517601.2:c.2425A>T	XP_011515903.1:p.Arg809Ter
XM_011517602.2:c.2383A>T	XP_011515904.1:p.Arg795Ter
XM_011517603.2:c.2284A>T	XP_011515905.1:p.Arg762Ter
XM_011517607.2:c.2260A>T	XP_011515909.1:p.Arg754Ter
XM_011517609.2:c.1405A>T	XP_011515911.1:p.Arg469Ter
XM_011517611.3:c.565A>T	XP_011515913.1:p.Arg189Ter
XM_017013847.2:c.2389A>T	XP_016869336.1:p.Arg797Ter
XM_017013848.2:c.2365A>T	XP_016869337.1:p.Arg789Ter
XM_017013849.2:c.2326A>T	XP_016869338.1:p.Arg776Ter
XM_017013850.2:c.2284A>T	XP_016869339.1:p.Arg762Ter
XM_017013851.2:c.2137A>T	XP_016869340.1:p.Arg713Ter
XM_017013852.2:c.2131A>T	XP_016869341.1:p.Arg711Ter
XM_017013854.2:c.1933A>T	XP_016869343.1:p.Arg645Ter
XM_017013855.2:c.1699A>T	XP_016869344.1:p.Arg567Ter
XM_017013856.2:c.1606A>T	XP_016869345.1:p.Arg536Ter
XM_017013858.2:c.772A>T	XP_016869347.1:p.Arg258Ter
XM_024447278.1:c.2260A>T	XP_024303046.1:p.Arg754Ter
XM_024447279.1:c.2179A>T	XP_024303047.1:p.Arg727Ter
XM_024447281.1:c.1984A>T	XP_024303049.1:p.Arg662Ter
XM_024447282.1:c.1687A>T	XP_024303050.1:p.Arg563Ter
XM_024447283.1:c.1363A>T	XP_024303051.1:p.Arg455Ter
XM_024447284.1:c.925A>T	XP_024303052.1:p.Arg309Ter
NM_001363131.2:c.2179A>T	NP_001350060.1:p.Arg727Ter
NM_001363132.2:c.2065A>T	NP_001350061.1:p.Arg689Ter
NM_001363133.2:c.1984A>T	NP_001350062.1:p.Arg662Ter
NM_001291339.2:c.1210A>T	NP_001278268.1:p.Arg404Ter
NM_001382391.1:c.2260A>T MANE Select	NP_001369320.1:p.Arg754Ter