Canonical Allele Identifier: CA1998755568
Gene: NPAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108219998A= , CM000673.2:g.108219998A= GRCh38
NC_000011.9:g.108090725A= , CM000673.1:g.108090725A= GRCh37
NC_000011.8:g.107595935A= NCBI36
NG_009830.1:g.2167A= , LRG_135:g.2167A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278612.9:c.37+2502T= MANE Select ENSP00000278612.8:n.37+2502T=
ENST00000278612.8:c.37+2502T= ENSP00000278612.8:n.37+2502T=
ENST00000531384.1:c.37+2502T= ENSP00000433497.1:n.37+2502T=
ENST00000610253.5:n.137+2502T=
NM_002519.2:c.37+2502T= NP_002510.2:n.37+2502T=
XM_011542854.1:c.37+2502T= XP_011541156.1:n.37+2502T=
XM_011542855.1:c.37+2502T= XP_011541157.1:n.37+2502T=
NM_001321307.1:c.37+2502T= NP_001308236.1:n.37+2502T=
XM_011542854.2:c.37+2502T= XP_011541156.1:n.37+2502T=
NM_002519.3:c.37+2502T= MANE Select NP_002510.2:n.37+2502T=