Canonical Allele Identifier: CA645557571

Gene: NPM1

Linked Data

• COSMIC: COSM36089

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.171410544_171410545delinsCTGGCG , CM000667.2:g.171410544_171410545delinsCTGGCG	GRCh38
NC_000005.9:g.170837548_170837549delinsCTGGCG , CM000667.1:g.170837548_170837549delinsCTGGCG	GRCh37
NC_000005.8:g.170770153_170770154delinsCTGGCG	NCBI36
NG_016018.1:g.27841_27842delinsCTGGCG , LRG_458:g.27841_27842delinsCTGGCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000296930.10:c.864_865delinsCTGGCG MANE Select	ENSP00000296930.5:p.Trp288CysfsTer12
ENST00000518587.2:n.1058_1059delinsCTGGCG
ENST00000521260.2:n.1242_1243delinsCTGGCG
ENST00000521672.6:c.672_673delinsCTGGCG	ENSP00000429485.2:p.Trp224CysfsTer12
ENST00000676504.1:n.1610_1611delinsCTGGCG
ENST00000676589.1:c.951_952delinsCTGGCG	ENSP00000503283.1:p.Trp317CysfsTer12
ENST00000676613.1:c.*1611_*1612delinsCTGGCG	ENSP00000503767.1:n.*1611_*1612delinsCTGGCG
ENST00000676625.1:n.3281_3282delinsCTGGCG
ENST00000677297.1:c.351_352delinsCTGGCG	ENSP00000504016.1:p.Trp117CysfsTer12
ENST00000677325.1:c.672_673delinsCTGGCG	ENSP00000503781.1:p.Trp224CysfsTer12
ENST00000677357.1:c.897_898delinsCTGGCG	ENSP00000504740.1:p.Trp299CysfsTer12
ENST00000677467.1:n.2289_2290delinsCTGGCG
ENST00000677600.1:n.2182_2183delinsCTGGCG
ENST00000677672.1:n.2287_2288delinsCTGGCG
ENST00000677682.1:n.2194_2195delinsCTGGCG
ENST00000677741.1:n.2130_2131delinsCTGGCG
ENST00000677904.1:n.1140_1141delinsCTGGCG
ENST00000677907.1:c.585_586delinsCTGGCG	ENSP00000504308.1:p.Trp195CysfsTer12
ENST00000678186.1:n.2334_2335delinsCTGGCG
ENST00000678267.1:c.*1965_*1966delinsCTGGCG	ENSP00000504107.1:n.*1965_*1966delinsCTGGCG
ENST00000678280.1:c.*849_*850delinsCTGGCG	ENSP00000503235.1:n.*849_*850delinsCTGGCG
ENST00000678774.1:c.*340_*341delinsCTGGCG	ENSP00000503150.1:n.*340_*341delinsCTGGCG
ENST00000679190.1:c.*47_*48delinsCTGGCG	ENSP00000503408.1:n.*47_*48delinsCTGGCG
ENST00000296930.9:c.864_865delinsCTGGCG	ENSP00000296930.5:p.Trp288CysfsTer12
ENST00000351986.10:c.777_778delinsCTGGCG	ENSP00000341168.6:p.Trp259CysfsTer12
ENST00000517671.5:c.864_865delinsCTGGCG	ENSP00000428755.1:p.Trp288CysfsTer12
ENST00000524204.1:n.300_301delinsCTGGCG
NM_002520.6:c.864_865delinsCTGGCG , LRG_458t1:c.864_865delinsCTGGCG	NP_002511.1:p.Trp288CysfsTer12
NM_199185.3:c.777_778delinsCTGGCG	NP_954654.1:p.Trp259CysfsTer12
XM_011534564.1:c.672_673delinsCTGGCG	XP_011532866.1:p.Trp224CysfsTer12
NM_001355006.1:c.864_865delinsCTGGCG	NP_001341935.1:p.Trp288CysfsTer12
NM_001355007.1:c.672_673delinsCTGGCG	NP_001341936.1:p.Trp224CysfsTer12
NM_001355010.1:c.483_484delinsCTGGCG	NP_001341939.1:p.Trp161CysfsTer12
NR_149149.1:n.981_982delinsCTGGCG
NM_001355006.2:c.864_865delinsCTGGCG	NP_001341935.1:p.Trp288CysfsTer12
NM_001355007.2:c.672_673delinsCTGGCG	NP_001341936.1:p.Trp224CysfsTer12
NM_001355010.2:c.483_484delinsCTGGCG	NP_001341939.1:p.Trp161CysfsTer12
NM_002520.7:c.864_865delinsCTGGCG MANE Select	NP_002511.1:p.Trp288CysfsTer12
NM_199185.4:c.777_778delinsCTGGCG	NP_954654.1:p.Trp259CysfsTer12
NR_149149.2:n.836_837delinsCTGGCG