Canonical Allele Identifier: CA371190638

Gene: CSPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.67159138G>T , CM000670.2:g.67159138G>T	GRCh38
NC_000008.10:g.68071373G>T , CM000670.1:g.68071373G>T	GRCh37
NC_000008.9:g.68233927G>T	NCBI36
NG_034100.1:g.99771G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001382391.1:c.2538+1G>T MANE Select	NP_001369320.1:n.2538+1G>T
ENST00000678616.1:c.2538+1G>T MANE Select	ENSP00000504733.1:n.2538+1G>T
NM_001291339.1:c.1488+1G>T	NP_001278268.1:n.1488+1G>T
NM_001291339.2:c.1488+1G>T	NP_001278268.1:n.1488+1G>T
NM_001363131.1:c.2457+1G>T	NP_001350060.1:n.2457+1G>T
NM_001363131.2:c.2457+1G>T	NP_001350060.1:n.2457+1G>T
NM_001363132.1:c.2343+1G>T	NP_001350061.1:n.2343+1G>T
NM_001363132.2:c.2343+1G>T	NP_001350061.1:n.2343+1G>T
NM_001363133.1:c.2262+1G>T	NP_001350062.1:n.2262+1G>T
NM_001363133.2:c.2262+1G>T	NP_001350062.1:n.2262+1G>T
NM_001364869.1:c.2604+1G>T	NP_001351798.1:n.2604+1G>T
NM_001364870.1:c.2424+1G>T	NP_001351799.1:n.2424+1G>T
NM_024790.6:c.2523+1G>T	NP_079066.5:n.2523+1G>T
ENST00000262210.11:c.2604+1G>T	ENSP00000262210.6:n.2604+1G>T
ENST00000262210.9:c.2523+1G>T	ENSP00000262210.5:n.2523+1G>T
ENST00000519668.1:c.1488+1G>T	ENSP00000430092.1:n.1488+1G>T
ENST00000521168.5:n.528+1G>T
ENST00000521324.3:c.410+1G>T
ENST00000674993.1:c.2628+1G>T	ENSP00000502454.1:n.2628+1G>T
ENST00000675306.2:c.2262+1G>T	ENSP00000502421.1:n.2262+1G>T
ENST00000675869.1:c.2343+1G>T	ENSP00000502747.1:n.2343+1G>T
ENST00000675955.1:c.2457+1G>T	ENSP00000501676.1:n.2457+1G>T
ENST00000675990.1:n.3867+1G>T
ENST00000676113.1:c.2496+1G>T	ENSP00000501645.1:n.2496+1G>T
ENST00000676317.1:c.2523+1G>T	ENSP00000502047.1:n.2523+1G>T
ENST00000676471.1:c.2271+1G>T	ENSP00000503711.1:n.2271+1G>T
ENST00000676573.1:c.1839+1G>T	ENSP00000504532.1:n.1839+1G>T
ENST00000676605.1:c.2646+1G>T	ENSP00000503605.1:n.2646+1G>T
ENST00000676804.1:c.841+1G>T
ENST00000676847.1:c.2517+1G>T	ENSP00000503336.1:n.2517+1G>T
ENST00000676858.1:c.*499+1G>T	ENSP00000502925.1:n.*499+1G>T
ENST00000676882.1:c.2424+1G>T	ENSP00000504342.1:n.2424+1G>T
ENST00000676968.1:c.410+1G>T
ENST00000677009.1:c.2523+1G>T	ENSP00000503297.1:n.2523+1G>T
ENST00000677052.1:n.2036+1G>T
ENST00000677131.1:c.410+1G>T
ENST00000677256.1:c.*2257+1G>T	ENSP00000504102.1:n.*2257+1G>T
ENST00000677430.1:c.*130+1G>T	ENSP00000504177.1:n.*130+1G>T
ENST00000677455.1:n.2411+1G>T
ENST00000677473.1:c.*554+1G>T	ENSP00000503534.1:n.*554+1G>T
ENST00000677592.1:c.2505+1G>T	ENSP00000504516.1:n.2505+1G>T
ENST00000677619.1:c.1884+1G>T	ENSP00000504522.1:n.1884+1G>T
ENST00000677697.1:n.501+1G>T
ENST00000677845.1:c.*909+1G>T	ENSP00000503524.1:n.*909+1G>T
ENST00000677855.1:c.1846+1G>T	ENSP00000504757.1:n.1846+1G>T
ENST00000677964.1:c.410+1G>T
ENST00000678017.1:c.1389+1G>T	ENSP00000504394.1:n.1389+1G>T
ENST00000678156.1:n.2178+1G>T
ENST00000678318.1:c.2073+1G>T	ENSP00000503690.1:n.2073+1G>T
ENST00000678542.1:c.2646+1G>T	ENSP00000503878.1:n.2646+1G>T
ENST00000678635.1:n.1033+1G>T
ENST00000678645.1:c.2415+1G>T	ENSP00000504031.1:n.2415+1G>T
ENST00000678723.1:c.410+1G>T
ENST00000678747.1:c.1965+1G>T	ENSP00000503390.1:n.1965+1G>T
ENST00000678895.1:c.410+1G>T
ENST00000679112.1:c.*2437+1G>T	ENSP00000503739.1:n.*2437+1G>T
ENST00000679226.1:c.2262+1G>T	ENSP00000503601.1:n.2262+1G>T
ENST00000679274.1:n.1462+1G>T
ENST00000679295.1:n.1509+1G>T
XM_005251305.3:c.2766+1G>T	XP_005251362.2:n.2766+1G>T
XM_005251305.4:c.2766+1G>T	XP_005251362.2:n.2766+1G>T
XM_006716474.2:c.2613+1G>T	XP_006716537.2:n.2613+1G>T
XM_006716474.3:c.2613+1G>T	XP_006716537.2:n.2613+1G>T
XM_006716477.2:c.2235+1G>T	XP_006716540.2:n.2235+1G>T
XM_006716477.3:c.2235+1G>T	XP_006716540.2:n.2235+1G>T
XM_011517598.1:c.2808+1G>T	XP_011515900.1:n.2808+1G>T
XM_011517598.2:c.2808+1G>T	XP_011515900.1:n.2808+1G>T
XM_011517599.1:c.2784+1G>T	XP_011515901.1:n.2784+1G>T
XM_011517599.2:c.2784+1G>T	XP_011515901.1:n.2784+1G>T
XM_011517600.1:c.2742+1G>T	XP_011515902.1:n.2742+1G>T
XM_011517600.2:c.2742+1G>T	XP_011515902.1:n.2742+1G>T
XM_011517601.1:c.2703+1G>T	XP_011515903.1:n.2703+1G>T
XM_011517601.2:c.2703+1G>T	XP_011515903.1:n.2703+1G>T
XM_011517602.1:c.2661+1G>T	XP_011515904.1:n.2661+1G>T
XM_011517602.2:c.2661+1G>T	XP_011515904.1:n.2661+1G>T
XM_011517603.1:c.2562+1G>T	XP_011515905.1:n.2562+1G>T
XM_011517603.2:c.2562+1G>T	XP_011515905.1:n.2562+1G>T
XM_011517604.1:c.2562+1G>T	XP_011515906.1:n.2562+1G>T
XM_011517605.1:c.2562+1G>T	XP_011515907.1:n.2562+1G>T
XM_011517606.1:c.2538+1G>T	XP_011515908.1:n.2538+1G>T
XM_011517607.1:c.2538+1G>T	XP_011515909.1:n.2538+1G>T
XM_011517607.2:c.2538+1G>T	XP_011515909.1:n.2538+1G>T
XM_011517608.1:c.2457+1G>T	XP_011515910.1:n.2457+1G>T
XM_011517609.1:c.1683+1G>T	XP_011515911.1:n.1683+1G>T
XM_011517609.2:c.1683+1G>T	XP_011515911.1:n.1683+1G>T
XM_011517610.1:c.1203+1G>T	XP_011515912.1:n.1203+1G>T
XM_011517611.1:c.843+1G>T	XP_011515913.1:n.843+1G>T
XM_011517611.3:c.843+1G>T	XP_011515913.1:n.843+1G>T
XM_017013847.2:c.2667+1G>T	XP_016869336.1:n.2667+1G>T
XM_017013848.2:c.2643+1G>T	XP_016869337.1:n.2643+1G>T
XM_017013849.2:c.2604+1G>T	XP_016869338.1:n.2604+1G>T
XM_017013850.2:c.2562+1G>T	XP_016869339.1:n.2562+1G>T
XM_017013851.2:c.2415+1G>T	XP_016869340.1:n.2415+1G>T
XM_017013852.2:c.2409+1G>T	XP_016869341.1:n.2409+1G>T
XM_017013854.2:c.2211+1G>T	XP_016869343.1:n.2211+1G>T
XM_017013855.2:c.1977+1G>T	XP_016869344.1:n.1977+1G>T
XM_017013856.2:c.1884+1G>T	XP_016869345.1:n.1884+1G>T
XM_017013858.2:c.1050+1G>T	XP_016869347.1:n.1050+1G>T
XM_024447278.1:c.2538+1G>T	XP_024303046.1:n.2538+1G>T
XM_024447279.1:c.2457+1G>T	XP_024303047.1:n.2457+1G>T
XM_024447281.1:c.2262+1G>T	XP_024303049.1:n.2262+1G>T
XM_024447282.1:c.1965+1G>T	XP_024303050.1:n.1965+1G>T
XM_024447283.1:c.1641+1G>T	XP_024303051.1:n.1641+1G>T
XM_024447284.1:c.1203+1G>T	XP_024303052.1:n.1203+1G>T