Canonical Allele Identifier: CA132111789

Gene: NPM1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.171392502C>A , CM000667.2:g.171392502C>A	GRCh38
NC_000005.9:g.170819506C>A , CM000667.1:g.170819506C>A	GRCh37
NC_000005.8:g.170752111C>A	NCBI36
NG_016018.1:g.9799C>A , LRG_458:g.9799C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296930.10:c.353-208C>A MANE Select	ENSP00000296930.5:n.353-208C>A
ENST00000518587.2:n.450-208C>A
ENST00000521260.2:n.731-208C>A
ENST00000521672.6:c.161-208C>A	ENSP00000429485.2:n.161-208C>A
ENST00000676504.1:n.471-208C>A
ENST00000676589.1:c.353-208C>A	ENSP00000503283.1:n.353-208C>A
ENST00000676613.1:c.353-208C>A	ENSP00000503767.1:n.353-208C>A
ENST00000676625.1:n.474-208C>A
ENST00000677297.1:c.258+1078C>A	ENSP00000504016.1:n.258+1078C>A
ENST00000677325.1:c.161-208C>A	ENSP00000503781.1:n.161-208C>A
ENST00000677357.1:c.353-208C>A	ENSP00000504740.1:n.353-208C>A
ENST00000677467.1:n.475-208C>A
ENST00000677600.1:n.368-208C>A
ENST00000677672.1:n.473-208C>A
ENST00000677741.1:n.1619-208C>A
ENST00000677904.1:n.629-208C>A
ENST00000677907.1:c.161-208C>A	ENSP00000504308.1:n.161-208C>A
ENST00000678186.1:n.607-208C>A
ENST00000678267.1:c.*238-208C>A	ENSP00000504107.1:n.*238-208C>A
ENST00000678280.1:c.353-208C>A	ENSP00000503235.1:n.353-208C>A
ENST00000678774.1:c.353-208C>A	ENSP00000503150.1:n.353-208C>A
ENST00000679006.1:n.474-208C>A
ENST00000679190.1:c.246+1090C>A	ENSP00000503408.1:n.246+1090C>A
ENST00000679233.1:c.353-208C>A	ENSP00000503717.1:n.353-208C>A
ENST00000296930.9:c.353-208C>A	ENSP00000296930.5:n.353-208C>A
ENST00000351986.10:c.353-208C>A	ENSP00000341168.6:n.353-208C>A
ENST00000393820.2:c.353-208C>A	ENSP00000377408.2:n.353-208C>A
ENST00000517671.5:c.353-208C>A	ENSP00000428755.1:n.353-208C>A
ENST00000518587.1:n.417-208C>A
ENST00000521672.5:c.161-208C>A	ENSP00000429485.1:n.161-208C>A
NM_001037738.2:c.353-208C>A	NP_001032827.1:n.353-208C>A
NM_002520.6:c.353-208C>A , LRG_458t1:c.353-208C>A	NP_002511.1:n.353-208C>A
NM_199185.3:c.353-208C>A	NP_954654.1:n.353-208C>A
XM_005265920.2:c.353-208C>A	XP_005265977.1:n.353-208C>A
XM_011534564.1:c.161-208C>A	XP_011532866.1:n.161-208C>A
NM_001355006.1:c.353-208C>A	NP_001341935.1:n.353-208C>A
NM_001355007.1:c.161-208C>A	NP_001341936.1:n.161-208C>A
NM_001355009.1:c.353-208C>A	NP_001341938.1:n.353-208C>A
NM_001355010.1:c.59-208C>A	NP_001341939.1:n.59-208C>A
NR_149149.1:n.598-208C>A
NM_001037738.3:c.353-208C>A	NP_001032827.1:n.353-208C>A
NM_001355009.2:c.353-208C>A	NP_001341938.1:n.353-208C>A
NM_001355006.2:c.353-208C>A	NP_001341935.1:n.353-208C>A
NM_001355007.2:c.161-208C>A	NP_001341936.1:n.161-208C>A
NM_001355010.2:c.59-208C>A	NP_001341939.1:n.59-208C>A
NM_002520.7:c.353-208C>A MANE Select	NP_002511.1:n.353-208C>A
NM_199185.4:c.353-208C>A	NP_954654.1:n.353-208C>A
NR_149149.2:n.453-208C>A