Canonical Allele Identifier: CA371188416

Gene: CSPP1

Linked Data

• MyVariant Identifiers: chr8:g.68070708A>T (hg19) ; chr8:g.67158473A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.67158473A>T , CM000670.2:g.67158473A>T	GRCh38
NC_000008.10:g.68070708A>T , CM000670.1:g.68070708A>T	GRCh37
NC_000008.9:g.68233262A>T	NCBI36
NG_034100.1:g.99106A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262210.11:c.2334A>T	ENSP00000262210.6:p.Glu778Asp
ENST00000521324.3:c.140A>T
ENST00000674993.1:c.2358A>T	ENSP00000502454.1:p.Glu786Asp
ENST00000675306.2:c.1992A>T	ENSP00000502421.1:p.Glu664Asp
ENST00000675869.1:c.2073A>T	ENSP00000502747.1:p.Glu691Asp
ENST00000675955.1:c.2187A>T	ENSP00000501676.1:p.Glu729Asp
ENST00000675990.1:n.3597A>T
ENST00000676113.1:c.2226A>T	ENSP00000501645.1:p.Glu742Asp
ENST00000676317.1:c.2253A>T	ENSP00000502047.1:p.Glu751Asp
ENST00000676471.1:c.2001A>T	ENSP00000503711.1:p.Glu667Asp
ENST00000676534.1:n.5194A>T
ENST00000676567.1:c.*892A>T	ENSP00000503427.1:n.*892A>T
ENST00000676573.1:c.1569A>T	ENSP00000504532.1:p.Glu523Asp
ENST00000676605.1:c.2376A>T	ENSP00000503605.1:p.Glu792Asp
ENST00000676695.1:c.2194A>T	ENSP00000503292.1:n.2194A>T
ENST00000676697.1:n.3129A>T
ENST00000676804.1:c.571A>T
ENST00000676847.1:c.2247A>T	ENSP00000503336.1:p.Glu749Asp
ENST00000676858.1:c.*229A>T	ENSP00000502925.1:n.*229A>T
ENST00000676882.1:c.2154A>T	ENSP00000504342.1:p.Glu718Asp
ENST00000676968.1:c.140A>T
ENST00000677009.1:c.2253A>T	ENSP00000503297.1:p.Glu751Asp
ENST00000677052.1:n.1766A>T
ENST00000677131.1:c.140A>T
ENST00000677256.1:c.*1987A>T	ENSP00000504102.1:n.*1987A>T
ENST00000677430.1:c.2187A>T	ENSP00000504177.1:p.Glu729Asp
ENST00000677455.1:n.2141A>T
ENST00000677473.1:c.*284A>T	ENSP00000503534.1:n.*284A>T
ENST00000677592.1:c.2235A>T	ENSP00000504516.1:p.Glu745Asp
ENST00000677619.1:c.1614A>T	ENSP00000504522.1:p.Glu538Asp
ENST00000677697.1:n.236A>T
ENST00000677845.1:c.*639A>T	ENSP00000503524.1:n.*639A>T
ENST00000677855.1:c.1576A>T	ENSP00000504757.1:n.1576A>T
ENST00000677964.1:c.140A>T
ENST00000678017.1:c.1119A>T	ENSP00000504394.1:p.Glu373Asp
ENST00000678138.1:n.2431A>T
ENST00000678156.1:n.1908A>T
ENST00000678318.1:c.1803A>T	ENSP00000503690.1:p.Glu601Asp
ENST00000678362.1:c.*1045A>T	ENSP00000504317.1:n.*1045A>T
ENST00000678542.1:c.2376A>T	ENSP00000503878.1:p.Glu792Asp
ENST00000678616.1:c.2268A>T MANE Select	ENSP00000504733.1:p.Glu756Asp
ENST00000678635.1:n.763A>T
ENST00000678645.1:c.2145A>T	ENSP00000504031.1:p.Glu715Asp
ENST00000678723.1:c.140A>T
ENST00000678747.1:c.1695A>T	ENSP00000503390.1:p.Glu565Asp
ENST00000678807.1:n.1303A>T
ENST00000678895.1:c.140A>T
ENST00000679042.1:n.3093A>T
ENST00000679112.1:c.*2167A>T	ENSP00000503739.1:n.*2167A>T
ENST00000679226.1:c.1992A>T	ENSP00000503601.1:p.Glu664Asp
ENST00000679274.1:n.1192A>T
ENST00000679295.1:n.1239A>T
ENST00000262210.9:c.2253A>T	ENSP00000262210.5:p.Glu751Asp
ENST00000519163.6:c.*2519A>T	ENSP00000428694.1:n.*2519A>T
ENST00000519668.1:c.1218A>T	ENSP00000430092.1:p.Glu406Asp
ENST00000521168.5:n.258A>T
NM_001291339.1:c.1218A>T	NP_001278268.1:p.Glu406Asp
NM_024790.6:c.2253A>T	NP_079066.5:p.Glu751Asp
XM_005251305.3:c.2496A>T	XP_005251362.2:p.Glu832Asp
XM_006716474.2:c.2343A>T	XP_006716537.2:p.Glu781Asp
XM_006716477.2:c.1965A>T	XP_006716540.2:p.Glu655Asp
XM_011517598.1:c.2538A>T	XP_011515900.1:p.Glu846Asp
XM_011517599.1:c.2514A>T	XP_011515901.1:p.Glu838Asp
XM_011517600.1:c.2472A>T	XP_011515902.1:p.Glu824Asp
XM_011517601.1:c.2433A>T	XP_011515903.1:p.Glu811Asp
XM_011517602.1:c.2391A>T	XP_011515904.1:p.Glu797Asp
XM_011517603.1:c.2292A>T	XP_011515905.1:p.Glu764Asp
XM_011517604.1:c.2292A>T	XP_011515906.1:p.Glu764Asp
XM_011517605.1:c.2292A>T	XP_011515907.1:p.Glu764Asp
XM_011517606.1:c.2268A>T	XP_011515908.1:p.Glu756Asp
XM_011517607.1:c.2268A>T	XP_011515909.1:p.Glu756Asp
XM_011517608.1:c.2187A>T	XP_011515910.1:p.Glu729Asp
XM_011517609.1:c.1413A>T	XP_011515911.1:p.Glu471Asp
XM_011517610.1:c.933A>T	XP_011515912.1:p.Glu311Asp
XM_011517611.1:c.573A>T	XP_011515913.1:p.Glu191Asp
NM_001363131.1:c.2187A>T	NP_001350060.1:p.Glu729Asp
NM_001363132.1:c.2073A>T	NP_001350061.1:p.Glu691Asp
NM_001363133.1:c.1992A>T	NP_001350062.1:p.Glu664Asp
NM_001364869.1:c.2334A>T	NP_001351798.1:p.Glu778Asp
NM_001364870.1:c.2154A>T	NP_001351799.1:p.Glu718Asp
XM_005251305.4:c.2496A>T	XP_005251362.2:p.Glu832Asp
XM_006716474.3:c.2343A>T	XP_006716537.2:p.Glu781Asp
XM_006716477.3:c.1965A>T	XP_006716540.2:p.Glu655Asp
XM_011517598.2:c.2538A>T	XP_011515900.1:p.Glu846Asp
XM_011517599.2:c.2514A>T	XP_011515901.1:p.Glu838Asp
XM_011517600.2:c.2472A>T	XP_011515902.1:p.Glu824Asp
XM_011517601.2:c.2433A>T	XP_011515903.1:p.Glu811Asp
XM_011517602.2:c.2391A>T	XP_011515904.1:p.Glu797Asp
XM_011517603.2:c.2292A>T	XP_011515905.1:p.Glu764Asp
XM_011517607.2:c.2268A>T	XP_011515909.1:p.Glu756Asp
XM_011517609.2:c.1413A>T	XP_011515911.1:p.Glu471Asp
XM_011517611.3:c.573A>T	XP_011515913.1:p.Glu191Asp
XM_017013847.2:c.2397A>T	XP_016869336.1:p.Glu799Asp
XM_017013848.2:c.2373A>T	XP_016869337.1:p.Glu791Asp
XM_017013849.2:c.2334A>T	XP_016869338.1:p.Glu778Asp
XM_017013850.2:c.2292A>T	XP_016869339.1:p.Glu764Asp
XM_017013851.2:c.2145A>T	XP_016869340.1:p.Glu715Asp
XM_017013852.2:c.2139A>T	XP_016869341.1:p.Glu713Asp
XM_017013854.2:c.1941A>T	XP_016869343.1:p.Glu647Asp
XM_017013855.2:c.1707A>T	XP_016869344.1:p.Glu569Asp
XM_017013856.2:c.1614A>T	XP_016869345.1:p.Glu538Asp
XM_017013858.2:c.780A>T	XP_016869347.1:p.Glu260Asp
XM_024447278.1:c.2268A>T	XP_024303046.1:p.Glu756Asp
XM_024447279.1:c.2187A>T	XP_024303047.1:p.Glu729Asp
XM_024447281.1:c.1992A>T	XP_024303049.1:p.Glu664Asp
XM_024447282.1:c.1695A>T	XP_024303050.1:p.Glu565Asp
XM_024447283.1:c.1371A>T	XP_024303051.1:p.Glu457Asp
XM_024447284.1:c.933A>T	XP_024303052.1:p.Glu311Asp
NM_001363131.2:c.2187A>T	NP_001350060.1:p.Glu729Asp
NM_001363132.2:c.2073A>T	NP_001350061.1:p.Glu691Asp
NM_001363133.2:c.1992A>T	NP_001350062.1:p.Glu664Asp
NM_001291339.2:c.1218A>T	NP_001278268.1:p.Glu406Asp
NM_001382391.1:c.2268A>T MANE Select	NP_001369320.1:p.Glu756Asp