Canonical Allele Identifier: CA371188403

Gene: CSPP1

Linked Data

• MyVariant Identifiers: chr8:g.68070705G>C (hg19) ; chr8:g.67158470G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.67158470G>C , CM000670.2:g.67158470G>C	GRCh38
NC_000008.10:g.68070705G>C , CM000670.1:g.68070705G>C	GRCh37
NC_000008.9:g.68233259G>C	NCBI36
NG_034100.1:g.99103G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262210.11:c.2331G>C	ENSP00000262210.6:p.Glu777Asp
ENST00000521324.3:c.137G>C
ENST00000674993.1:c.2355G>C	ENSP00000502454.1:p.Glu785Asp
ENST00000675306.2:c.1989G>C	ENSP00000502421.1:p.Glu663Asp
ENST00000675869.1:c.2070G>C	ENSP00000502747.1:p.Glu690Asp
ENST00000675955.1:c.2184G>C	ENSP00000501676.1:p.Glu728Asp
ENST00000675990.1:n.3594G>C
ENST00000676113.1:c.2223G>C	ENSP00000501645.1:p.Glu741Asp
ENST00000676317.1:c.2250G>C	ENSP00000502047.1:p.Glu750Asp
ENST00000676471.1:c.1998G>C	ENSP00000503711.1:p.Glu666Asp
ENST00000676534.1:n.5191G>C
ENST00000676567.1:c.*889G>C	ENSP00000503427.1:n.*889G>C
ENST00000676573.1:c.1566G>C	ENSP00000504532.1:p.Glu522Asp
ENST00000676605.1:c.2373G>C	ENSP00000503605.1:p.Glu791Asp
ENST00000676695.1:c.2191G>C	ENSP00000503292.1:n.2191G>C
ENST00000676697.1:n.3126G>C
ENST00000676804.1:c.568G>C
ENST00000676847.1:c.2244G>C	ENSP00000503336.1:p.Glu748Asp
ENST00000676858.1:c.*226G>C	ENSP00000502925.1:n.*226G>C
ENST00000676882.1:c.2151G>C	ENSP00000504342.1:p.Glu717Asp
ENST00000676968.1:c.137G>C
ENST00000677009.1:c.2250G>C	ENSP00000503297.1:p.Glu750Asp
ENST00000677052.1:n.1763G>C
ENST00000677131.1:c.137G>C
ENST00000677256.1:c.*1984G>C	ENSP00000504102.1:n.*1984G>C
ENST00000677430.1:c.2184G>C	ENSP00000504177.1:p.Glu728Asp
ENST00000677455.1:n.2138G>C
ENST00000677473.1:c.*281G>C	ENSP00000503534.1:n.*281G>C
ENST00000677592.1:c.2232G>C	ENSP00000504516.1:p.Glu744Asp
ENST00000677619.1:c.1611G>C	ENSP00000504522.1:p.Glu537Asp
ENST00000677697.1:n.233G>C
ENST00000677845.1:c.*636G>C	ENSP00000503524.1:n.*636G>C
ENST00000677855.1:c.1573G>C	ENSP00000504757.1:n.1573G>C
ENST00000677964.1:c.137G>C
ENST00000678017.1:c.1116G>C	ENSP00000504394.1:p.Glu372Asp
ENST00000678138.1:n.2428G>C
ENST00000678156.1:n.1905G>C
ENST00000678318.1:c.1800G>C	ENSP00000503690.1:p.Glu600Asp
ENST00000678362.1:c.*1042G>C	ENSP00000504317.1:n.*1042G>C
ENST00000678542.1:c.2373G>C	ENSP00000503878.1:p.Glu791Asp
ENST00000678616.1:c.2265G>C MANE Select	ENSP00000504733.1:p.Glu755Asp
ENST00000678635.1:n.760G>C
ENST00000678645.1:c.2142G>C	ENSP00000504031.1:p.Glu714Asp
ENST00000678723.1:c.137G>C
ENST00000678747.1:c.1692G>C	ENSP00000503390.1:p.Glu564Asp
ENST00000678807.1:n.1300G>C
ENST00000678895.1:c.137G>C
ENST00000679042.1:n.3090G>C
ENST00000679112.1:c.*2164G>C	ENSP00000503739.1:n.*2164G>C
ENST00000679226.1:c.1989G>C	ENSP00000503601.1:p.Glu663Asp
ENST00000679274.1:n.1189G>C
ENST00000679295.1:n.1236G>C
ENST00000262210.9:c.2250G>C	ENSP00000262210.5:p.Glu750Asp
ENST00000519163.6:c.*2516G>C	ENSP00000428694.1:n.*2516G>C
ENST00000519668.1:c.1215G>C	ENSP00000430092.1:p.Glu405Asp
ENST00000521168.5:n.255G>C
NM_001291339.1:c.1215G>C	NP_001278268.1:p.Glu405Asp
NM_024790.6:c.2250G>C	NP_079066.5:p.Glu750Asp
XM_005251305.3:c.2493G>C	XP_005251362.2:p.Glu831Asp
XM_006716474.2:c.2340G>C	XP_006716537.2:p.Glu780Asp
XM_006716477.2:c.1962G>C	XP_006716540.2:p.Glu654Asp
XM_011517598.1:c.2535G>C	XP_011515900.1:p.Glu845Asp
XM_011517599.1:c.2511G>C	XP_011515901.1:p.Glu837Asp
XM_011517600.1:c.2469G>C	XP_011515902.1:p.Glu823Asp
XM_011517601.1:c.2430G>C	XP_011515903.1:p.Glu810Asp
XM_011517602.1:c.2388G>C	XP_011515904.1:p.Glu796Asp
XM_011517603.1:c.2289G>C	XP_011515905.1:p.Glu763Asp
XM_011517604.1:c.2289G>C	XP_011515906.1:p.Glu763Asp
XM_011517605.1:c.2289G>C	XP_011515907.1:p.Glu763Asp
XM_011517606.1:c.2265G>C	XP_011515908.1:p.Glu755Asp
XM_011517607.1:c.2265G>C	XP_011515909.1:p.Glu755Asp
XM_011517608.1:c.2184G>C	XP_011515910.1:p.Glu728Asp
XM_011517609.1:c.1410G>C	XP_011515911.1:p.Glu470Asp
XM_011517610.1:c.930G>C	XP_011515912.1:p.Glu310Asp
XM_011517611.1:c.570G>C	XP_011515913.1:p.Glu190Asp
NM_001363131.1:c.2184G>C	NP_001350060.1:p.Glu728Asp
NM_001363132.1:c.2070G>C	NP_001350061.1:p.Glu690Asp
NM_001363133.1:c.1989G>C	NP_001350062.1:p.Glu663Asp
NM_001364869.1:c.2331G>C	NP_001351798.1:p.Glu777Asp
NM_001364870.1:c.2151G>C	NP_001351799.1:p.Glu717Asp
XM_005251305.4:c.2493G>C	XP_005251362.2:p.Glu831Asp
XM_006716474.3:c.2340G>C	XP_006716537.2:p.Glu780Asp
XM_006716477.3:c.1962G>C	XP_006716540.2:p.Glu654Asp
XM_011517598.2:c.2535G>C	XP_011515900.1:p.Glu845Asp
XM_011517599.2:c.2511G>C	XP_011515901.1:p.Glu837Asp
XM_011517600.2:c.2469G>C	XP_011515902.1:p.Glu823Asp
XM_011517601.2:c.2430G>C	XP_011515903.1:p.Glu810Asp
XM_011517602.2:c.2388G>C	XP_011515904.1:p.Glu796Asp
XM_011517603.2:c.2289G>C	XP_011515905.1:p.Glu763Asp
XM_011517607.2:c.2265G>C	XP_011515909.1:p.Glu755Asp
XM_011517609.2:c.1410G>C	XP_011515911.1:p.Glu470Asp
XM_011517611.3:c.570G>C	XP_011515913.1:p.Glu190Asp
XM_017013847.2:c.2394G>C	XP_016869336.1:p.Glu798Asp
XM_017013848.2:c.2370G>C	XP_016869337.1:p.Glu790Asp
XM_017013849.2:c.2331G>C	XP_016869338.1:p.Glu777Asp
XM_017013850.2:c.2289G>C	XP_016869339.1:p.Glu763Asp
XM_017013851.2:c.2142G>C	XP_016869340.1:p.Glu714Asp
XM_017013852.2:c.2136G>C	XP_016869341.1:p.Glu712Asp
XM_017013854.2:c.1938G>C	XP_016869343.1:p.Glu646Asp
XM_017013855.2:c.1704G>C	XP_016869344.1:p.Glu568Asp
XM_017013856.2:c.1611G>C	XP_016869345.1:p.Glu537Asp
XM_017013858.2:c.777G>C	XP_016869347.1:p.Glu259Asp
XM_024447278.1:c.2265G>C	XP_024303046.1:p.Glu755Asp
XM_024447279.1:c.2184G>C	XP_024303047.1:p.Glu728Asp
XM_024447281.1:c.1989G>C	XP_024303049.1:p.Glu663Asp
XM_024447282.1:c.1692G>C	XP_024303050.1:p.Glu564Asp
XM_024447283.1:c.1368G>C	XP_024303051.1:p.Glu456Asp
XM_024447284.1:c.930G>C	XP_024303052.1:p.Glu310Asp
NM_001363131.2:c.2184G>C	NP_001350060.1:p.Glu728Asp
NM_001363132.2:c.2070G>C	NP_001350061.1:p.Glu690Asp
NM_001363133.2:c.1989G>C	NP_001350062.1:p.Glu663Asp
NM_001291339.2:c.1215G>C	NP_001278268.1:p.Glu405Asp
NM_001382391.1:c.2265G>C MANE Select	NP_001369320.1:p.Glu755Asp