Canonical Allele Identifier: CA371188419

Gene: CSPP1

Linked Data

• MyVariant Identifiers: chr8:g.68070709G>C (hg19) ; chr8:g.67158474G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.67158474G>C , CM000670.2:g.67158474G>C	GRCh38
NC_000008.10:g.68070709G>C , CM000670.1:g.68070709G>C	GRCh37
NC_000008.9:g.68233263G>C	NCBI36
NG_034100.1:g.99107G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262210.11:c.2335G>C	ENSP00000262210.6:p.Ala779Pro
ENST00000521324.3:c.141G>C
ENST00000674993.1:c.2359G>C	ENSP00000502454.1:p.Ala787Pro
ENST00000675306.2:c.1993G>C	ENSP00000502421.1:p.Ala665Pro
ENST00000675869.1:c.2074G>C	ENSP00000502747.1:p.Ala692Pro
ENST00000675955.1:c.2188G>C	ENSP00000501676.1:p.Ala730Pro
ENST00000675990.1:n.3598G>C
ENST00000676113.1:c.2227G>C	ENSP00000501645.1:p.Ala743Pro
ENST00000676317.1:c.2254G>C	ENSP00000502047.1:p.Ala752Pro
ENST00000676471.1:c.2002G>C	ENSP00000503711.1:p.Ala668Pro
ENST00000676534.1:n.5195G>C
ENST00000676567.1:c.*893G>C	ENSP00000503427.1:n.*893G>C
ENST00000676573.1:c.1570G>C	ENSP00000504532.1:p.Ala524Pro
ENST00000676605.1:c.2377G>C	ENSP00000503605.1:p.Ala793Pro
ENST00000676695.1:c.2195G>C	ENSP00000503292.1:n.2195G>C
ENST00000676697.1:n.3130G>C
ENST00000676804.1:c.572G>C
ENST00000676847.1:c.2248G>C	ENSP00000503336.1:p.Ala750Pro
ENST00000676858.1:c.*230G>C	ENSP00000502925.1:n.*230G>C
ENST00000676882.1:c.2155G>C	ENSP00000504342.1:p.Ala719Pro
ENST00000676968.1:c.141G>C
ENST00000677009.1:c.2254G>C	ENSP00000503297.1:p.Ala752Pro
ENST00000677052.1:n.1767G>C
ENST00000677131.1:c.141G>C
ENST00000677256.1:c.*1988G>C	ENSP00000504102.1:n.*1988G>C
ENST00000677430.1:c.2188G>C	ENSP00000504177.1:p.Ala730Pro
ENST00000677455.1:n.2142G>C
ENST00000677473.1:c.*285G>C	ENSP00000503534.1:n.*285G>C
ENST00000677592.1:c.2236G>C	ENSP00000504516.1:p.Ala746Pro
ENST00000677619.1:c.1615G>C	ENSP00000504522.1:p.Ala539Pro
ENST00000677697.1:n.237G>C
ENST00000677845.1:c.*640G>C	ENSP00000503524.1:n.*640G>C
ENST00000677855.1:c.1577G>C	ENSP00000504757.1:n.1577G>C
ENST00000677964.1:c.141G>C
ENST00000678017.1:c.1120G>C	ENSP00000504394.1:p.Ala374Pro
ENST00000678138.1:n.2432G>C
ENST00000678156.1:n.1909G>C
ENST00000678318.1:c.1804G>C	ENSP00000503690.1:p.Ala602Pro
ENST00000678362.1:c.*1046G>C	ENSP00000504317.1:n.*1046G>C
ENST00000678542.1:c.2377G>C	ENSP00000503878.1:p.Ala793Pro
ENST00000678616.1:c.2269G>C MANE Select	ENSP00000504733.1:p.Ala757Pro
ENST00000678635.1:n.764G>C
ENST00000678645.1:c.2146G>C	ENSP00000504031.1:p.Ala716Pro
ENST00000678723.1:c.141G>C
ENST00000678747.1:c.1696G>C	ENSP00000503390.1:p.Ala566Pro
ENST00000678807.1:n.1304G>C
ENST00000678895.1:c.141G>C
ENST00000679042.1:n.3094G>C
ENST00000679112.1:c.*2168G>C	ENSP00000503739.1:n.*2168G>C
ENST00000679226.1:c.1993G>C	ENSP00000503601.1:p.Ala665Pro
ENST00000679274.1:n.1193G>C
ENST00000679295.1:n.1240G>C
ENST00000262210.9:c.2254G>C	ENSP00000262210.5:p.Ala752Pro
ENST00000519163.6:c.*2520G>C	ENSP00000428694.1:n.*2520G>C
ENST00000519668.1:c.1219G>C	ENSP00000430092.1:p.Ala407Pro
ENST00000521168.5:n.259G>C
NM_001291339.1:c.1219G>C	NP_001278268.1:p.Ala407Pro
NM_024790.6:c.2254G>C	NP_079066.5:p.Ala752Pro
XM_005251305.3:c.2497G>C	XP_005251362.2:p.Ala833Pro
XM_006716474.2:c.2344G>C	XP_006716537.2:p.Ala782Pro
XM_006716477.2:c.1966G>C	XP_006716540.2:p.Ala656Pro
XM_011517598.1:c.2539G>C	XP_011515900.1:p.Ala847Pro
XM_011517599.1:c.2515G>C	XP_011515901.1:p.Ala839Pro
XM_011517600.1:c.2473G>C	XP_011515902.1:p.Ala825Pro
XM_011517601.1:c.2434G>C	XP_011515903.1:p.Ala812Pro
XM_011517602.1:c.2392G>C	XP_011515904.1:p.Ala798Pro
XM_011517603.1:c.2293G>C	XP_011515905.1:p.Ala765Pro
XM_011517604.1:c.2293G>C	XP_011515906.1:p.Ala765Pro
XM_011517605.1:c.2293G>C	XP_011515907.1:p.Ala765Pro
XM_011517606.1:c.2269G>C	XP_011515908.1:p.Ala757Pro
XM_011517607.1:c.2269G>C	XP_011515909.1:p.Ala757Pro
XM_011517608.1:c.2188G>C	XP_011515910.1:p.Ala730Pro
XM_011517609.1:c.1414G>C	XP_011515911.1:p.Ala472Pro
XM_011517610.1:c.934G>C	XP_011515912.1:p.Ala312Pro
XM_011517611.1:c.574G>C	XP_011515913.1:p.Ala192Pro
NM_001363131.1:c.2188G>C	NP_001350060.1:p.Ala730Pro
NM_001363132.1:c.2074G>C	NP_001350061.1:p.Ala692Pro
NM_001363133.1:c.1993G>C	NP_001350062.1:p.Ala665Pro
NM_001364869.1:c.2335G>C	NP_001351798.1:p.Ala779Pro
NM_001364870.1:c.2155G>C	NP_001351799.1:p.Ala719Pro
XM_005251305.4:c.2497G>C	XP_005251362.2:p.Ala833Pro
XM_006716474.3:c.2344G>C	XP_006716537.2:p.Ala782Pro
XM_006716477.3:c.1966G>C	XP_006716540.2:p.Ala656Pro
XM_011517598.2:c.2539G>C	XP_011515900.1:p.Ala847Pro
XM_011517599.2:c.2515G>C	XP_011515901.1:p.Ala839Pro
XM_011517600.2:c.2473G>C	XP_011515902.1:p.Ala825Pro
XM_011517601.2:c.2434G>C	XP_011515903.1:p.Ala812Pro
XM_011517602.2:c.2392G>C	XP_011515904.1:p.Ala798Pro
XM_011517603.2:c.2293G>C	XP_011515905.1:p.Ala765Pro
XM_011517607.2:c.2269G>C	XP_011515909.1:p.Ala757Pro
XM_011517609.2:c.1414G>C	XP_011515911.1:p.Ala472Pro
XM_011517611.3:c.574G>C	XP_011515913.1:p.Ala192Pro
XM_017013847.2:c.2398G>C	XP_016869336.1:p.Ala800Pro
XM_017013848.2:c.2374G>C	XP_016869337.1:p.Ala792Pro
XM_017013849.2:c.2335G>C	XP_016869338.1:p.Ala779Pro
XM_017013850.2:c.2293G>C	XP_016869339.1:p.Ala765Pro
XM_017013851.2:c.2146G>C	XP_016869340.1:p.Ala716Pro
XM_017013852.2:c.2140G>C	XP_016869341.1:p.Ala714Pro
XM_017013854.2:c.1942G>C	XP_016869343.1:p.Ala648Pro
XM_017013855.2:c.1708G>C	XP_016869344.1:p.Ala570Pro
XM_017013856.2:c.1615G>C	XP_016869345.1:p.Ala539Pro
XM_017013858.2:c.781G>C	XP_016869347.1:p.Ala261Pro
XM_024447278.1:c.2269G>C	XP_024303046.1:p.Ala757Pro
XM_024447279.1:c.2188G>C	XP_024303047.1:p.Ala730Pro
XM_024447281.1:c.1993G>C	XP_024303049.1:p.Ala665Pro
XM_024447282.1:c.1696G>C	XP_024303050.1:p.Ala566Pro
XM_024447283.1:c.1372G>C	XP_024303051.1:p.Ala458Pro
XM_024447284.1:c.934G>C	XP_024303052.1:p.Ala312Pro
NM_001363131.2:c.2188G>C	NP_001350060.1:p.Ala730Pro
NM_001363132.2:c.2074G>C	NP_001350061.1:p.Ala692Pro
NM_001363133.2:c.1993G>C	NP_001350062.1:p.Ala665Pro
NM_001291339.2:c.1219G>C	NP_001278268.1:p.Ala407Pro
NM_001382391.1:c.2269G>C MANE Select	NP_001369320.1:p.Ala757Pro