Canonical Allele Identifier: CA1998755577
Gene: NPAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108220008G= , CM000673.2:g.108220008G= GRCh38
NC_000011.9:g.108090735G= , CM000673.1:g.108090735G= GRCh37
NC_000011.8:g.107595945G= NCBI36
NG_009830.1:g.2177G= , LRG_135:g.2177G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278612.9:c.37+2492C= MANE Select ENSP00000278612.8:n.37+2492C=
ENST00000278612.8:c.37+2492C= ENSP00000278612.8:n.37+2492C=
ENST00000531384.1:c.37+2492C= ENSP00000433497.1:n.37+2492C=
ENST00000610253.5:n.137+2492C=
NM_002519.2:c.37+2492C= NP_002510.2:n.37+2492C=
XM_011542854.1:c.37+2492C= XP_011541156.1:n.37+2492C=
XM_011542855.1:c.37+2492C= XP_011541157.1:n.37+2492C=
NM_001321307.1:c.37+2492C= NP_001308236.1:n.37+2492C=
XM_011542854.2:c.37+2492C= XP_011541156.1:n.37+2492C=
NM_002519.3:c.37+2492C= MANE Select NP_002510.2:n.37+2492C=