Canonical Allele Identifier: CA4770933
Community Standard Title: NM_001382391.1(CSPP1):c.2741C>G (p.Ser914Ter)
Gene: CSPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.67164421C>G , CM000670.2:g.67164421C>G GRCh38
NC_000008.10:g.68076656C>G , CM000670.1:g.68076656C>G GRCh37
NC_000008.9:g.68239210C>G NCBI36
NG_034100.1:g.105054C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001382391.1:c.2741C>G MANE Select NP_001369320.1:p.Ser914Ter
ENST00000678616.1:c.2741C>G MANE Select ENSP00000504733.1:p.Ser914Ter
NM_001291339.1:c.1691C>G NP_001278268.1:p.Ser564Ter
NM_001291339.2:c.1691C>G NP_001278268.1:p.Ser564Ter
NM_001363131.1:c.2660C>G NP_001350060.1:p.Ser887Ter
NM_001363131.2:c.2660C>G NP_001350060.1:p.Ser887Ter
NM_001363132.1:c.2546C>G NP_001350061.1:p.Ser849Ter
NM_001363132.2:c.2546C>G NP_001350061.1:p.Ser849Ter
NM_001363133.1:c.2465C>G NP_001350062.1:p.Ser822Ter
NM_001363133.2:c.2465C>G NP_001350062.1:p.Ser822Ter
NM_001364869.1:c.2807C>G NP_001351798.1:p.Ser936Ter
NM_001364870.1:c.2627C>G NP_001351799.1:p.Ser876Ter
NM_024790.6:c.2726C>G NP_079066.5:p.Ser909Ter
ENST00000262210.11:c.2807C>G ENSP00000262210.6:p.Ser936Ter
ENST00000262210.9:c.2726C>G ENSP00000262210.5:p.Ser909Ter
ENST00000519668.1:c.1691C>G ENSP00000430092.1:p.Ser564Ter
ENST00000521168.5:n.731C>G
ENST00000521324.3:c.613C>G
ENST00000674993.1:c.2831C>G ENSP00000502454.1:p.Ser944Ter
ENST00000675306.2:c.2465C>G ENSP00000502421.1:p.Ser822Ter
ENST00000675869.1:c.2546C>G ENSP00000502747.1:p.Ser849Ter
ENST00000675955.1:c.2660C>G ENSP00000501676.1:p.Ser887Ter
ENST00000675990.1:n.4070C>G
ENST00000676113.1:c.2699C>G ENSP00000501645.1:p.Ser900Ter
ENST00000676317.1:c.2726C>G ENSP00000502047.1:p.Ser909Ter
ENST00000676471.1:c.2474C>G ENSP00000503711.1:p.Ser825Ter
ENST00000676573.1:c.2042C>G ENSP00000504532.1:p.Ser681Ter
ENST00000676605.1:c.2849C>G ENSP00000503605.1:p.Ser950Ter
ENST00000676804.1:c.1044C>G
ENST00000676847.1:c.2720C>G ENSP00000503336.1:p.Ser907Ter
ENST00000676858.1:c.*702C>G ENSP00000502925.1:n.*702C>G
ENST00000676882.1:c.2627C>G ENSP00000504342.1:p.Ser876Ter
ENST00000676968.1:c.613C>G
ENST00000677009.1:c.2726C>G ENSP00000503297.1:p.Ser909Ter
ENST00000677052.1:n.2239C>G
ENST00000677131.1:c.613C>G
ENST00000677256.1:c.*2460C>G ENSP00000504102.1:n.*2460C>G
ENST00000677430.1:c.*333C>G ENSP00000504177.1:n.*333C>G
ENST00000677473.1:c.*757C>G ENSP00000503534.1:n.*757C>G
ENST00000677592.1:c.2708C>G ENSP00000504516.1:p.Ser903Ter
ENST00000677619.1:c.2087C>G ENSP00000504522.1:p.Ser696Ter
ENST00000677697.1:n.704C>G
ENST00000677845.1:c.*1112C>G ENSP00000503524.1:n.*1112C>G
ENST00000677855.1:c.2049C>G ENSP00000504757.1:n.2049C>G
ENST00000677964.1:c.738C>G
ENST00000678017.1:c.1592C>G ENSP00000504394.1:p.Ser531Ter
ENST00000678156.1:n.2381C>G
ENST00000678318.1:c.2276C>G ENSP00000503690.1:p.Ser759Ter
ENST00000678542.1:c.2849C>G ENSP00000503878.1:p.Ser950Ter
ENST00000678635.1:n.1236C>G
ENST00000678645.1:c.2618C>G ENSP00000504031.1:p.Ser873Ter
ENST00000678723.1:c.613C>G
ENST00000678747.1:c.2168C>G ENSP00000503390.1:p.Ser723Ter
ENST00000678895.1:c.613C>G
ENST00000679112.1:c.*2640C>G ENSP00000503739.1:n.*2640C>G
ENST00000679226.1:c.2465C>G ENSP00000503601.1:p.Ser822Ter
ENST00000679274.1:n.1665C>G
ENST00000679295.1:n.1712C>G
XM_005251305.3:c.2969C>G XP_005251362.2:p.Ser990Ter
XM_005251305.4:c.2969C>G XP_005251362.2:p.Ser990Ter
XM_006716474.2:c.2816C>G XP_006716537.2:p.Ser939Ter
XM_006716474.3:c.2816C>G XP_006716537.2:p.Ser939Ter
XM_006716477.2:c.2438C>G XP_006716540.2:p.Ser813Ter
XM_006716477.3:c.2438C>G XP_006716540.2:p.Ser813Ter
XM_011517598.1:c.3011C>G XP_011515900.1:p.Ser1004Ter
XM_011517598.2:c.3011C>G XP_011515900.1:p.Ser1004Ter
XM_011517599.1:c.2987C>G XP_011515901.1:p.Ser996Ter
XM_011517599.2:c.2987C>G XP_011515901.1:p.Ser996Ter
XM_011517600.1:c.2945C>G XP_011515902.1:p.Ser982Ter
XM_011517600.2:c.2945C>G XP_011515902.1:p.Ser982Ter
XM_011517601.1:c.2906C>G XP_011515903.1:p.Ser969Ter
XM_011517601.2:c.2906C>G XP_011515903.1:p.Ser969Ter
XM_011517602.1:c.2864C>G XP_011515904.1:p.Ser955Ter
XM_011517602.2:c.2864C>G XP_011515904.1:p.Ser955Ter
XM_011517603.1:c.2765C>G XP_011515905.1:p.Ser922Ter
XM_011517603.2:c.2765C>G XP_011515905.1:p.Ser922Ter
XM_011517604.1:c.2765C>G XP_011515906.1:p.Ser922Ter
XM_011517605.1:c.2765C>G XP_011515907.1:p.Ser922Ter
XM_011517606.1:c.2741C>G XP_011515908.1:p.Ser914Ter
XM_011517607.1:c.2741C>G XP_011515909.1:p.Ser914Ter
XM_011517607.2:c.2741C>G XP_011515909.1:p.Ser914Ter
XM_011517608.1:c.2660C>G XP_011515910.1:p.Ser887Ter
XM_011517609.1:c.1886C>G XP_011515911.1:p.Ser629Ter
XM_011517609.2:c.1886C>G XP_011515911.1:p.Ser629Ter
XM_011517610.1:c.1406C>G XP_011515912.1:p.Ser469Ter
XM_011517611.1:c.1046C>G XP_011515913.1:p.Ser349Ter
XM_011517611.3:c.1046C>G XP_011515913.1:p.Ser349Ter
XM_017013847.2:c.2870C>G XP_016869336.1:p.Ser957Ter
XM_017013848.2:c.2846C>G XP_016869337.1:p.Ser949Ter
XM_017013849.2:c.2807C>G XP_016869338.1:p.Ser936Ter
XM_017013850.2:c.2765C>G XP_016869339.1:p.Ser922Ter
XM_017013851.2:c.2618C>G XP_016869340.1:p.Ser873Ter
XM_017013852.2:c.2612C>G XP_016869341.1:p.Ser871Ter
XM_017013854.2:c.2414C>G XP_016869343.1:p.Ser805Ter
XM_017013855.2:c.2180C>G XP_016869344.1:p.Ser727Ter
XM_017013856.2:c.2087C>G XP_016869345.1:p.Ser696Ter
XM_017013858.2:c.1253C>G XP_016869347.1:p.Ser418Ter
XM_024447278.1:c.2741C>G XP_024303046.1:p.Ser914Ter
XM_024447279.1:c.2660C>G XP_024303047.1:p.Ser887Ter
XM_024447281.1:c.2465C>G XP_024303049.1:p.Ser822Ter
XM_024447282.1:c.2168C>G XP_024303050.1:p.Ser723Ter
XM_024447283.1:c.1844C>G XP_024303051.1:p.Ser615Ter
XM_024447284.1:c.1406C>G XP_024303052.1:p.Ser469Ter