Canonical Allele Identifier: CA1998755589
Gene: NPAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108220050A= , CM000673.2:g.108220050A= GRCh38
NC_000011.9:g.108090777A= , CM000673.1:g.108090777A= GRCh37
NC_000011.8:g.107595987A= NCBI36
NG_009830.1:g.2219A= , LRG_135:g.2219A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278612.9:c.37+2450T= MANE Select ENSP00000278612.8:n.37+2450T=
ENST00000278612.8:c.37+2450T= ENSP00000278612.8:n.37+2450T=
ENST00000531384.1:c.37+2450T= ENSP00000433497.1:n.37+2450T=
ENST00000610253.5:n.137+2450T=
NM_002519.2:c.37+2450T= NP_002510.2:n.37+2450T=
XM_011542854.1:c.37+2450T= XP_011541156.1:n.37+2450T=
XM_011542855.1:c.37+2450T= XP_011541157.1:n.37+2450T=
NM_001321307.1:c.37+2450T= NP_001308236.1:n.37+2450T=
XM_011542854.2:c.37+2450T= XP_011541156.1:n.37+2450T=
NM_002519.3:c.37+2450T= MANE Select NP_002510.2:n.37+2450T=