Canonical Allele Identifier: CA461295967

Gene: CSPP1

Linked Data

• MyVariant Identifiers: chr8:g.68070702A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.67158467A>G , CM000670.2:g.67158467A>G	GRCh38
NC_000008.10:g.68070702A>G , CM000670.1:g.68070702A>G	GRCh37
NC_000008.9:g.68233256A>G	NCBI36
NG_034100.1:g.99100A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000262210.11:c.2328A>G	ENSP00000262210.6:p.Arg776=
ENST00000521324.3:c.134A>G
ENST00000674993.1:c.2352A>G	ENSP00000502454.1:p.Arg784=
ENST00000675306.2:c.1986A>G	ENSP00000502421.1:p.Arg662=
ENST00000675869.1:c.2067A>G	ENSP00000502747.1:p.Arg689=
ENST00000675955.1:c.2181A>G	ENSP00000501676.1:p.Arg727=
ENST00000675990.1:n.3591A>G
ENST00000676113.1:c.2220A>G	ENSP00000501645.1:p.Arg740=
ENST00000676317.1:c.2247A>G	ENSP00000502047.1:p.Arg749=
ENST00000676471.1:c.1995A>G	ENSP00000503711.1:p.Arg665=
ENST00000676534.1:n.5188A>G
ENST00000676567.1:c.*886A>G	ENSP00000503427.1:n.*886A>G
ENST00000676573.1:c.1563A>G	ENSP00000504532.1:p.Arg521=
ENST00000676605.1:c.2370A>G	ENSP00000503605.1:p.Arg790=
ENST00000676695.1:c.2188A>G	ENSP00000503292.1:n.2188A>G
ENST00000676697.1:n.3123A>G
ENST00000676804.1:c.565A>G
ENST00000676847.1:c.2241A>G	ENSP00000503336.1:p.Arg747=
ENST00000676858.1:c.*223A>G	ENSP00000502925.1:n.*223A>G
ENST00000676882.1:c.2148A>G	ENSP00000504342.1:p.Arg716=
ENST00000676968.1:c.134A>G
ENST00000677009.1:c.2247A>G	ENSP00000503297.1:p.Arg749=
ENST00000677052.1:n.1760A>G
ENST00000677131.1:c.134A>G
ENST00000677256.1:c.*1981A>G	ENSP00000504102.1:n.*1981A>G
ENST00000677430.1:c.2181A>G	ENSP00000504177.1:p.Arg727=
ENST00000677455.1:n.2135A>G
ENST00000677473.1:c.*278A>G	ENSP00000503534.1:n.*278A>G
ENST00000677592.1:c.2229A>G	ENSP00000504516.1:p.Arg743=
ENST00000677619.1:c.1608A>G	ENSP00000504522.1:p.Arg536=
ENST00000677697.1:n.230A>G
ENST00000677845.1:c.*633A>G	ENSP00000503524.1:n.*633A>G
ENST00000677855.1:c.1570A>G	ENSP00000504757.1:n.1570A>G
ENST00000677964.1:c.134A>G
ENST00000678017.1:c.1113A>G	ENSP00000504394.1:p.Arg371=
ENST00000678138.1:n.2425A>G
ENST00000678156.1:n.1902A>G
ENST00000678318.1:c.1797A>G	ENSP00000503690.1:p.Arg599=
ENST00000678362.1:c.*1039A>G	ENSP00000504317.1:n.*1039A>G
ENST00000678542.1:c.2370A>G	ENSP00000503878.1:p.Arg790=
ENST00000678616.1:c.2262A>G MANE Select	ENSP00000504733.1:p.Arg754=
ENST00000678635.1:n.757A>G
ENST00000678645.1:c.2139A>G	ENSP00000504031.1:p.Arg713=
ENST00000678723.1:c.134A>G
ENST00000678747.1:c.1689A>G	ENSP00000503390.1:p.Arg563=
ENST00000678807.1:n.1297A>G
ENST00000678895.1:c.134A>G
ENST00000679042.1:n.3087A>G
ENST00000679112.1:c.*2161A>G	ENSP00000503739.1:n.*2161A>G
ENST00000679226.1:c.1986A>G	ENSP00000503601.1:p.Arg662=
ENST00000679274.1:n.1186A>G
ENST00000679295.1:n.1233A>G
ENST00000262210.9:c.2247A>G	ENSP00000262210.5:p.Arg749=
ENST00000519163.6:c.*2513A>G	ENSP00000428694.1:n.*2513A>G
ENST00000519668.1:c.1212A>G	ENSP00000430092.1:p.Arg404=
ENST00000521168.5:n.252A>G
NM_001291339.1:c.1212A>G	NP_001278268.1:p.Arg404=
NM_024790.6:c.2247A>G	NP_079066.5:p.Arg749=
XM_005251305.3:c.2490A>G	XP_005251362.2:p.Arg830=
XM_006716474.2:c.2337A>G	XP_006716537.2:p.Arg779=
XM_006716477.2:c.1959A>G	XP_006716540.2:p.Arg653=
XM_011517598.1:c.2532A>G	XP_011515900.1:p.Arg844=
XM_011517599.1:c.2508A>G	XP_011515901.1:p.Arg836=
XM_011517600.1:c.2466A>G	XP_011515902.1:p.Arg822=
XM_011517601.1:c.2427A>G	XP_011515903.1:p.Arg809=
XM_011517602.1:c.2385A>G	XP_011515904.1:p.Arg795=
XM_011517603.1:c.2286A>G	XP_011515905.1:p.Arg762=
XM_011517604.1:c.2286A>G	XP_011515906.1:p.Arg762=
XM_011517605.1:c.2286A>G	XP_011515907.1:p.Arg762=
XM_011517606.1:c.2262A>G	XP_011515908.1:p.Arg754=
XM_011517607.1:c.2262A>G	XP_011515909.1:p.Arg754=
XM_011517608.1:c.2181A>G	XP_011515910.1:p.Arg727=
XM_011517609.1:c.1407A>G	XP_011515911.1:p.Arg469=
XM_011517610.1:c.927A>G	XP_011515912.1:p.Arg309=
XM_011517611.1:c.567A>G	XP_011515913.1:p.Arg189=
NM_001363131.1:c.2181A>G	NP_001350060.1:p.Arg727=
NM_001363132.1:c.2067A>G	NP_001350061.1:p.Arg689=
NM_001363133.1:c.1986A>G	NP_001350062.1:p.Arg662=
NM_001364869.1:c.2328A>G	NP_001351798.1:p.Arg776=
NM_001364870.1:c.2148A>G	NP_001351799.1:p.Arg716=
XM_005251305.4:c.2490A>G	XP_005251362.2:p.Arg830=
XM_006716474.3:c.2337A>G	XP_006716537.2:p.Arg779=
XM_006716477.3:c.1959A>G	XP_006716540.2:p.Arg653=
XM_011517598.2:c.2532A>G	XP_011515900.1:p.Arg844=
XM_011517599.2:c.2508A>G	XP_011515901.1:p.Arg836=
XM_011517600.2:c.2466A>G	XP_011515902.1:p.Arg822=
XM_011517601.2:c.2427A>G	XP_011515903.1:p.Arg809=
XM_011517602.2:c.2385A>G	XP_011515904.1:p.Arg795=
XM_011517603.2:c.2286A>G	XP_011515905.1:p.Arg762=
XM_011517607.2:c.2262A>G	XP_011515909.1:p.Arg754=
XM_011517609.2:c.1407A>G	XP_011515911.1:p.Arg469=
XM_011517611.3:c.567A>G	XP_011515913.1:p.Arg189=
XM_017013847.2:c.2391A>G	XP_016869336.1:p.Arg797=
XM_017013848.2:c.2367A>G	XP_016869337.1:p.Arg789=
XM_017013849.2:c.2328A>G	XP_016869338.1:p.Arg776=
XM_017013850.2:c.2286A>G	XP_016869339.1:p.Arg762=
XM_017013851.2:c.2139A>G	XP_016869340.1:p.Arg713=
XM_017013852.2:c.2133A>G	XP_016869341.1:p.Arg711=
XM_017013854.2:c.1935A>G	XP_016869343.1:p.Arg645=
XM_017013855.2:c.1701A>G	XP_016869344.1:p.Arg567=
XM_017013856.2:c.1608A>G	XP_016869345.1:p.Arg536=
XM_017013858.2:c.774A>G	XP_016869347.1:p.Arg258=
XM_024447278.1:c.2262A>G	XP_024303046.1:p.Arg754=
XM_024447279.1:c.2181A>G	XP_024303047.1:p.Arg727=
XM_024447281.1:c.1986A>G	XP_024303049.1:p.Arg662=
XM_024447282.1:c.1689A>G	XP_024303050.1:p.Arg563=
XM_024447283.1:c.1365A>G	XP_024303051.1:p.Arg455=
XM_024447284.1:c.927A>G	XP_024303052.1:p.Arg309=
NM_001363131.2:c.2181A>G	NP_001350060.1:p.Arg727=
NM_001363132.2:c.2067A>G	NP_001350061.1:p.Arg689=
NM_001363133.2:c.1986A>G	NP_001350062.1:p.Arg662=
NM_001291339.2:c.1212A>G	NP_001278268.1:p.Arg404=
NM_001382391.1:c.2262A>G MANE Select	NP_001369320.1:p.Arg754=