Canonical Allele Identifier: CA371188424

Gene: CSPP1

Linked Data

• MyVariant Identifiers: chr8:g.68070710C>G (hg19) ; chr8:g.67158475C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.67158475C>G , CM000670.2:g.67158475C>G	GRCh38
NC_000008.10:g.68070710C>G , CM000670.1:g.68070710C>G	GRCh37
NC_000008.9:g.68233264C>G	NCBI36
NG_034100.1:g.99108C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262210.11:c.2336C>G	ENSP00000262210.6:p.Ala779Gly
ENST00000521324.3:c.142C>G
ENST00000674993.1:c.2360C>G	ENSP00000502454.1:p.Ala787Gly
ENST00000675306.2:c.1994C>G	ENSP00000502421.1:p.Ala665Gly
ENST00000675869.1:c.2075C>G	ENSP00000502747.1:p.Ala692Gly
ENST00000675955.1:c.2189C>G	ENSP00000501676.1:p.Ala730Gly
ENST00000675990.1:n.3599C>G
ENST00000676113.1:c.2228C>G	ENSP00000501645.1:p.Ala743Gly
ENST00000676317.1:c.2255C>G	ENSP00000502047.1:p.Ala752Gly
ENST00000676471.1:c.2003C>G	ENSP00000503711.1:p.Ala668Gly
ENST00000676534.1:n.5196C>G
ENST00000676567.1:c.*894C>G	ENSP00000503427.1:n.*894C>G
ENST00000676573.1:c.1571C>G	ENSP00000504532.1:p.Ala524Gly
ENST00000676605.1:c.2378C>G	ENSP00000503605.1:p.Ala793Gly
ENST00000676695.1:c.2196C>G	ENSP00000503292.1:n.2196C>G
ENST00000676697.1:n.3131C>G
ENST00000676804.1:c.573C>G
ENST00000676847.1:c.2249C>G	ENSP00000503336.1:p.Ala750Gly
ENST00000676858.1:c.*231C>G	ENSP00000502925.1:n.*231C>G
ENST00000676882.1:c.2156C>G	ENSP00000504342.1:p.Ala719Gly
ENST00000676968.1:c.142C>G
ENST00000677009.1:c.2255C>G	ENSP00000503297.1:p.Ala752Gly
ENST00000677052.1:n.1768C>G
ENST00000677131.1:c.142C>G
ENST00000677256.1:c.*1989C>G	ENSP00000504102.1:n.*1989C>G
ENST00000677430.1:c.2189C>G	ENSP00000504177.1:p.Ala730Gly
ENST00000677455.1:n.2143C>G
ENST00000677473.1:c.*286C>G	ENSP00000503534.1:n.*286C>G
ENST00000677592.1:c.2237C>G	ENSP00000504516.1:p.Ala746Gly
ENST00000677619.1:c.1616C>G	ENSP00000504522.1:p.Ala539Gly
ENST00000677697.1:n.238C>G
ENST00000677845.1:c.*641C>G	ENSP00000503524.1:n.*641C>G
ENST00000677855.1:c.1578C>G	ENSP00000504757.1:n.1578C>G
ENST00000677964.1:c.142C>G
ENST00000678017.1:c.1121C>G	ENSP00000504394.1:p.Ala374Gly
ENST00000678138.1:n.2433C>G
ENST00000678156.1:n.1910C>G
ENST00000678318.1:c.1805C>G	ENSP00000503690.1:p.Ala602Gly
ENST00000678362.1:c.*1047C>G	ENSP00000504317.1:n.*1047C>G
ENST00000678542.1:c.2378C>G	ENSP00000503878.1:p.Ala793Gly
ENST00000678616.1:c.2270C>G MANE Select	ENSP00000504733.1:p.Ala757Gly
ENST00000678635.1:n.765C>G
ENST00000678645.1:c.2147C>G	ENSP00000504031.1:p.Ala716Gly
ENST00000678723.1:c.142C>G
ENST00000678747.1:c.1697C>G	ENSP00000503390.1:p.Ala566Gly
ENST00000678807.1:n.1305C>G
ENST00000678895.1:c.142C>G
ENST00000679042.1:n.3095C>G
ENST00000679112.1:c.*2169C>G	ENSP00000503739.1:n.*2169C>G
ENST00000679226.1:c.1994C>G	ENSP00000503601.1:p.Ala665Gly
ENST00000679274.1:n.1194C>G
ENST00000679295.1:n.1241C>G
ENST00000262210.9:c.2255C>G	ENSP00000262210.5:p.Ala752Gly
ENST00000519163.6:c.*2521C>G	ENSP00000428694.1:n.*2521C>G
ENST00000519668.1:c.1220C>G	ENSP00000430092.1:p.Ala407Gly
ENST00000521168.5:n.260C>G
NM_001291339.1:c.1220C>G	NP_001278268.1:p.Ala407Gly
NM_024790.6:c.2255C>G	NP_079066.5:p.Ala752Gly
XM_005251305.3:c.2498C>G	XP_005251362.2:p.Ala833Gly
XM_006716474.2:c.2345C>G	XP_006716537.2:p.Ala782Gly
XM_006716477.2:c.1967C>G	XP_006716540.2:p.Ala656Gly
XM_011517598.1:c.2540C>G	XP_011515900.1:p.Ala847Gly
XM_011517599.1:c.2516C>G	XP_011515901.1:p.Ala839Gly
XM_011517600.1:c.2474C>G	XP_011515902.1:p.Ala825Gly
XM_011517601.1:c.2435C>G	XP_011515903.1:p.Ala812Gly
XM_011517602.1:c.2393C>G	XP_011515904.1:p.Ala798Gly
XM_011517603.1:c.2294C>G	XP_011515905.1:p.Ala765Gly
XM_011517604.1:c.2294C>G	XP_011515906.1:p.Ala765Gly
XM_011517605.1:c.2294C>G	XP_011515907.1:p.Ala765Gly
XM_011517606.1:c.2270C>G	XP_011515908.1:p.Ala757Gly
XM_011517607.1:c.2270C>G	XP_011515909.1:p.Ala757Gly
XM_011517608.1:c.2189C>G	XP_011515910.1:p.Ala730Gly
XM_011517609.1:c.1415C>G	XP_011515911.1:p.Ala472Gly
XM_011517610.1:c.935C>G	XP_011515912.1:p.Ala312Gly
XM_011517611.1:c.575C>G	XP_011515913.1:p.Ala192Gly
NM_001363131.1:c.2189C>G	NP_001350060.1:p.Ala730Gly
NM_001363132.1:c.2075C>G	NP_001350061.1:p.Ala692Gly
NM_001363133.1:c.1994C>G	NP_001350062.1:p.Ala665Gly
NM_001364869.1:c.2336C>G	NP_001351798.1:p.Ala779Gly
NM_001364870.1:c.2156C>G	NP_001351799.1:p.Ala719Gly
XM_005251305.4:c.2498C>G	XP_005251362.2:p.Ala833Gly
XM_006716474.3:c.2345C>G	XP_006716537.2:p.Ala782Gly
XM_006716477.3:c.1967C>G	XP_006716540.2:p.Ala656Gly
XM_011517598.2:c.2540C>G	XP_011515900.1:p.Ala847Gly
XM_011517599.2:c.2516C>G	XP_011515901.1:p.Ala839Gly
XM_011517600.2:c.2474C>G	XP_011515902.1:p.Ala825Gly
XM_011517601.2:c.2435C>G	XP_011515903.1:p.Ala812Gly
XM_011517602.2:c.2393C>G	XP_011515904.1:p.Ala798Gly
XM_011517603.2:c.2294C>G	XP_011515905.1:p.Ala765Gly
XM_011517607.2:c.2270C>G	XP_011515909.1:p.Ala757Gly
XM_011517609.2:c.1415C>G	XP_011515911.1:p.Ala472Gly
XM_011517611.3:c.575C>G	XP_011515913.1:p.Ala192Gly
XM_017013847.2:c.2399C>G	XP_016869336.1:p.Ala800Gly
XM_017013848.2:c.2375C>G	XP_016869337.1:p.Ala792Gly
XM_017013849.2:c.2336C>G	XP_016869338.1:p.Ala779Gly
XM_017013850.2:c.2294C>G	XP_016869339.1:p.Ala765Gly
XM_017013851.2:c.2147C>G	XP_016869340.1:p.Ala716Gly
XM_017013852.2:c.2141C>G	XP_016869341.1:p.Ala714Gly
XM_017013854.2:c.1943C>G	XP_016869343.1:p.Ala648Gly
XM_017013855.2:c.1709C>G	XP_016869344.1:p.Ala570Gly
XM_017013856.2:c.1616C>G	XP_016869345.1:p.Ala539Gly
XM_017013858.2:c.782C>G	XP_016869347.1:p.Ala261Gly
XM_024447278.1:c.2270C>G	XP_024303046.1:p.Ala757Gly
XM_024447279.1:c.2189C>G	XP_024303047.1:p.Ala730Gly
XM_024447281.1:c.1994C>G	XP_024303049.1:p.Ala665Gly
XM_024447282.1:c.1697C>G	XP_024303050.1:p.Ala566Gly
XM_024447283.1:c.1373C>G	XP_024303051.1:p.Ala458Gly
XM_024447284.1:c.935C>G	XP_024303052.1:p.Ala312Gly
NM_001363131.2:c.2189C>G	NP_001350060.1:p.Ala730Gly
NM_001363132.2:c.2075C>G	NP_001350061.1:p.Ala692Gly
NM_001363133.2:c.1994C>G	NP_001350062.1:p.Ala665Gly
NM_001291339.2:c.1220C>G	NP_001278268.1:p.Ala407Gly
NM_001382391.1:c.2270C>G MANE Select	NP_001369320.1:p.Ala757Gly