Canonical Allele Identifier: CA1998755566
Gene: NPAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108219994T= , CM000673.2:g.108219994T= GRCh38
NC_000011.9:g.108090721T= , CM000673.1:g.108090721T= GRCh37
NC_000011.8:g.107595931T= NCBI36
NG_009830.1:g.2163T= , LRG_135:g.2163T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278612.9:c.37+2506A= MANE Select ENSP00000278612.8:n.37+2506A=
ENST00000278612.8:c.37+2506A= ENSP00000278612.8:n.37+2506A=
ENST00000531384.1:c.37+2506A= ENSP00000433497.1:n.37+2506A=
ENST00000610253.5:n.137+2506A=
NM_002519.2:c.37+2506A= NP_002510.2:n.37+2506A=
XM_011542854.1:c.37+2506A= XP_011541156.1:n.37+2506A=
XM_011542855.1:c.37+2506A= XP_011541157.1:n.37+2506A=
NM_001321307.1:c.37+2506A= NP_001308236.1:n.37+2506A=
XM_011542854.2:c.37+2506A= XP_011541156.1:n.37+2506A=
NM_002519.3:c.37+2506A= MANE Select NP_002510.2:n.37+2506A=