Canonical Allele Identifier: CA1998755592

Gene: NPAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108220059_108220061delinsATG , CM000673.2:g.108220059_108220061delinsATG	GRCh38
NC_000011.9:g.108090786_108090788delinsATG , CM000673.1:g.108090786_108090788delinsATG	GRCh37
NC_000011.8:g.107595996_107595998delinsATG	NCBI36
NG_009830.1:g.2228_2230delinsATG , LRG_135:g.2228_2230delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278612.9:c.37+2439_37+2441delinsCAT MANE Select	ENSP00000278612.8:n.37+2439_37+2441delinsCAT
ENST00000278612.8:c.37+2439_37+2441delinsCAT	ENSP00000278612.8:n.37+2439_37+2441delinsCAT
ENST00000531384.1:c.37+2439_37+2441delinsCAT	ENSP00000433497.1:n.37+2439_37+2441delinsCAT
ENST00000610253.5:n.137+2439_137+2441delinsCAT
NM_002519.2:c.37+2439_37+2441delinsCAT	NP_002510.2:n.37+2439_37+2441delinsCAT
XM_011542854.1:c.37+2439_37+2441delinsCAT	XP_011541156.1:n.37+2439_37+2441delinsCAT
XM_011542855.1:c.37+2439_37+2441delinsCAT	XP_011541157.1:n.37+2439_37+2441delinsCAT
NM_001321307.1:c.37+2439_37+2441delinsCAT	NP_001308236.1:n.37+2439_37+2441delinsCAT
XM_011542854.2:c.37+2439_37+2441delinsCAT	XP_011541156.1:n.37+2439_37+2441delinsCAT
NM_002519.3:c.37+2439_37+2441delinsCAT MANE Select	NP_002510.2:n.37+2439_37+2441delinsCAT