Canonical Allele Identifier: CA2568682564

Gene: NPAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108220213_108220220del , CM000673.2:g.108220213_108220220del	GRCh38
NC_000011.9:g.108090940_108090947del , CM000673.1:g.108090940_108090947del	GRCh37
NC_000011.8:g.107596150_107596157del	NCBI36
NG_009830.1:g.2382_2389del , LRG_135:g.2382_2389del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278612.9:c.37+2284_37+2291del MANE Select	ENSP00000278612.8:n.37+2284_37+2291del
ENST00000278612.8:c.37+2284_37+2291del	ENSP00000278612.8:n.37+2284_37+2291del
ENST00000531384.1:c.37+2284_37+2291del	ENSP00000433497.1:n.37+2284_37+2291del
ENST00000610253.5:n.137+2284_137+2291del
NM_002519.2:c.37+2284_37+2291del	NP_002510.2:n.37+2284_37+2291del
XM_011542854.1:c.37+2284_37+2291del	XP_011541156.1:n.37+2284_37+2291del
XM_011542855.1:c.37+2284_37+2291del	XP_011541157.1:n.37+2284_37+2291del
NM_001321307.1:c.37+2284_37+2291del	NP_001308236.1:n.37+2284_37+2291del
XM_011542854.2:c.37+2284_37+2291del	XP_011541156.1:n.37+2284_37+2291del
NM_002519.3:c.37+2284_37+2291del MANE Select	NP_002510.2:n.37+2284_37+2291del