Canonical Allele Identifier: CA2497030032

Gene: NPM1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.171410541_171410545delinsTTCCAGGCT , CM000667.2:g.171410541_171410545delinsTTCCAGGCT	GRCh38
NC_000005.9:g.170837545_170837549delinsTTCCAGGCT , CM000667.1:g.170837545_170837549delinsTTCCAGGCT	GRCh37
NC_000005.8:g.170770150_170770154delinsTTCCAGGCT	NCBI36
NG_016018.1:g.27838_27842delinsTTCCAGGCT , LRG_458:g.27838_27842delinsTTCCAGGCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000296930.10:c.861_865delinsTTCCAGGCT MANE Select	ENSP00000296930.5:p.Trp288SerfsTer12
ENST00000518587.2:n.1055_1059delinsTTCCAGGCT
ENST00000521260.2:n.1239_1243delinsTTCCAGGCT
ENST00000521672.6:c.669_673delinsTTCCAGGCT	ENSP00000429485.2:p.Trp224SerfsTer12
ENST00000676504.1:n.1607_1611delinsTTCCAGGCT
ENST00000676589.1:c.948_952delinsTTCCAGGCT	ENSP00000503283.1:p.Trp317SerfsTer12
ENST00000676613.1:c.*1608_*1612delinsTTCCAGGCT	ENSP00000503767.1:n.*1608_*1612delinsTTCCAGGCT
ENST00000676625.1:n.3278_3282delinsTTCCAGGCT
ENST00000677297.1:c.348_352delinsTTCCAGGCT	ENSP00000504016.1:p.Trp117SerfsTer12
ENST00000677325.1:c.669_673delinsTTCCAGGCT	ENSP00000503781.1:p.Trp224SerfsTer12
ENST00000677357.1:c.894_898delinsTTCCAGGCT	ENSP00000504740.1:p.Trp299SerfsTer12
ENST00000677467.1:n.2286_2290delinsTTCCAGGCT
ENST00000677600.1:n.2179_2183delinsTTCCAGGCT
ENST00000677672.1:n.2284_2288delinsTTCCAGGCT
ENST00000677682.1:n.2191_2195delinsTTCCAGGCT
ENST00000677741.1:n.2127_2131delinsTTCCAGGCT
ENST00000677904.1:n.1137_1141delinsTTCCAGGCT
ENST00000677907.1:c.582_586delinsTTCCAGGCT	ENSP00000504308.1:p.Trp195SerfsTer12
ENST00000678186.1:n.2331_2335delinsTTCCAGGCT
ENST00000678267.1:c.*1962_*1966delinsTTCCAGGCT	ENSP00000504107.1:n.*1962_*1966delinsTTCCAGGCT
ENST00000678280.1:c.*846_*850delinsTTCCAGGCT	ENSP00000503235.1:n.*846_*850delinsTTCCAGGCT
ENST00000678774.1:c.*337_*341delinsTTCCAGGCT	ENSP00000503150.1:n.*337_*341delinsTTCCAGGCT
ENST00000679190.1:c.*44_*48delinsTTCCAGGCT	ENSP00000503408.1:n.*44_*48delinsTTCCAGGCT
ENST00000296930.9:c.861_865delinsTTCCAGGCT	ENSP00000296930.5:p.Trp288SerfsTer12
ENST00000351986.10:c.774_778delinsTTCCAGGCT	ENSP00000341168.6:p.Trp259SerfsTer12
ENST00000517671.5:c.861_865delinsTTCCAGGCT	ENSP00000428755.1:p.Trp288SerfsTer12
ENST00000524204.1:n.297_301delinsTTCCAGGCT
NM_002520.6:c.861_865delinsTTCCAGGCT , LRG_458t1:c.861_865delinsTTCCAGGCT	NP_002511.1:p.Trp288SerfsTer12
NM_199185.3:c.774_778delinsTTCCAGGCT	NP_954654.1:p.Trp259SerfsTer12
XM_011534564.1:c.669_673delinsTTCCAGGCT	XP_011532866.1:p.Trp224SerfsTer12
NM_001355006.1:c.861_865delinsTTCCAGGCT	NP_001341935.1:p.Trp288SerfsTer12
NM_001355007.1:c.669_673delinsTTCCAGGCT	NP_001341936.1:p.Trp224SerfsTer12
NM_001355010.1:c.480_484delinsTTCCAGGCT	NP_001341939.1:p.Trp161SerfsTer12
NR_149149.1:n.978_982delinsTTCCAGGCT
NM_001355006.2:c.861_865delinsTTCCAGGCT	NP_001341935.1:p.Trp288SerfsTer12
NM_001355007.2:c.669_673delinsTTCCAGGCT	NP_001341936.1:p.Trp224SerfsTer12
NM_001355010.2:c.480_484delinsTTCCAGGCT	NP_001341939.1:p.Trp161SerfsTer12
NM_002520.7:c.861_865delinsTTCCAGGCT MANE Select	NP_002511.1:p.Trp288SerfsTer12
NM_199185.4:c.774_778delinsTTCCAGGCT	NP_954654.1:p.Trp259SerfsTer12
NR_149149.2:n.833_837delinsTTCCAGGCT