Canonical Allele Identifier: CA1084359429

Gene: NPM1

Linked Data

• gnomAD v3: 5-171410542-TGGCA-T
• gnomAD v4: 5-171410542-TGGCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.171410544_171410547del , CM000667.2:g.171410544_171410547del	GRCh38
NC_000005.9:g.170837548_170837551del , CM000667.1:g.170837548_170837551del	GRCh37
NC_000005.8:g.170770153_170770156del	NCBI36
NG_016018.1:g.27841_27844del , LRG_458:g.27841_27844del

Transcript Alleles

HGVS	Amino-acid change
ENST00000296930.10:c.864_867del MANE Select	ENSP00000296930.5:p.Trp288CysfsTer11
ENST00000518587.2:n.1058_1061del
ENST00000521260.2:n.1242_1245del
ENST00000521672.6:c.672_675del	ENSP00000429485.2:p.Trp224CysfsTer11
ENST00000676504.1:n.1610_1613del
ENST00000676589.1:c.951_954del	ENSP00000503283.1:p.Trp317CysfsTer11
ENST00000676613.1:c.*1611_*1614del	ENSP00000503767.1:n.*1611_*1614del
ENST00000676625.1:n.3281_3284del
ENST00000677297.1:c.351_354del	ENSP00000504016.1:p.Trp117CysfsTer11
ENST00000677325.1:c.672_675del	ENSP00000503781.1:p.Trp224CysfsTer11
ENST00000677357.1:c.897_900del	ENSP00000504740.1:p.Trp299CysfsTer11
ENST00000677467.1:n.2289_2292del
ENST00000677600.1:n.2182_2185del
ENST00000677672.1:n.2287_2290del
ENST00000677682.1:n.2194_2197del
ENST00000677741.1:n.2130_2133del
ENST00000677904.1:n.1140_1143del
ENST00000677907.1:c.585_588del	ENSP00000504308.1:p.Trp195CysfsTer11
ENST00000678186.1:n.2334_2337del
ENST00000678267.1:c.*1965_*1968del	ENSP00000504107.1:n.*1965_*1968del
ENST00000678280.1:c.*849_*852del	ENSP00000503235.1:n.*849_*852del
ENST00000678774.1:c.*340_*343del	ENSP00000503150.1:n.*340_*343del
ENST00000679190.1:c.*47_*50del	ENSP00000503408.1:n.*47_*50del
ENST00000296930.9:c.864_867del	ENSP00000296930.5:p.Trp288CysfsTer11
ENST00000351986.10:c.777_780del	ENSP00000341168.6:p.Trp259CysfsTer11
ENST00000517671.5:c.864_867del	ENSP00000428755.1:p.Trp288CysfsTer11
ENST00000524204.1:n.300_303del
NM_002520.6:c.864_867del , LRG_458t1:c.864_867del	NP_002511.1:p.Trp288CysfsTer11
NM_199185.3:c.777_780del	NP_954654.1:p.Trp259CysfsTer11
XM_011534564.1:c.672_675del	XP_011532866.1:p.Trp224CysfsTer11
NM_001355006.1:c.864_867del	NP_001341935.1:p.Trp288CysfsTer11
NM_001355007.1:c.672_675del	NP_001341936.1:p.Trp224CysfsTer11
NM_001355010.1:c.483_486del	NP_001341939.1:p.Trp161CysfsTer11
NR_149149.1:n.981_984del
NM_001355006.2:c.864_867del	NP_001341935.1:p.Trp288CysfsTer11
NM_001355007.2:c.672_675del	NP_001341936.1:p.Trp224CysfsTer11
NM_001355010.2:c.483_486del	NP_001341939.1:p.Trp161CysfsTer11
NM_002520.7:c.864_867del MANE Select	NP_002511.1:p.Trp288CysfsTer11
NM_199185.4:c.777_780del	NP_954654.1:p.Trp259CysfsTer11
NR_149149.2:n.836_839del