Canonical Allele Identifier: CA2527994089

Gene: NPAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108219764_108219765del , CM000673.2:g.108219764_108219765del	GRCh38
NC_000011.9:g.108090491_108090492del , CM000673.1:g.108090491_108090492del	GRCh37
NC_000011.8:g.107595701_107595702del	NCBI36
NG_009830.1:g.1933_1934del , LRG_135:g.1933_1934del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278612.9:c.37+2736_37+2737del MANE Select	ENSP00000278612.8:n.37+2736_37+2737del
ENST00000278612.8:c.37+2736_37+2737del	ENSP00000278612.8:n.37+2736_37+2737del
ENST00000531384.1:c.37+2736_37+2737del	ENSP00000433497.1:n.37+2736_37+2737del
ENST00000610253.5:n.137+2736_137+2737del
NM_002519.2:c.37+2736_37+2737del	NP_002510.2:n.37+2736_37+2737del
XM_011542854.1:c.37+2736_37+2737del	XP_011541156.1:n.37+2736_37+2737del
XM_011542855.1:c.37+2736_37+2737del	XP_011541157.1:n.37+2736_37+2737del
NM_001321307.1:c.37+2736_37+2737del	NP_001308236.1:n.37+2736_37+2737del
XM_011542854.2:c.37+2736_37+2737del	XP_011541156.1:n.37+2736_37+2737del
NM_002519.3:c.37+2736_37+2737del MANE Select	NP_002510.2:n.37+2736_37+2737del