Canonical Allele Identifier: CA1998755446

Gene: NPAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108219736_108219738delinsAAC , CM000673.2:g.108219736_108219738delinsAAC	GRCh38
NC_000011.9:g.108090463_108090465delinsAAC , CM000673.1:g.108090463_108090465delinsAAC	GRCh37
NC_000011.8:g.107595673_107595675delinsAAC	NCBI36
NG_009830.1:g.1905_1907delinsAAC , LRG_135:g.1905_1907delinsAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278612.9:c.37+2762_37+2764delinsGTT MANE Select	ENSP00000278612.8:n.37+2762_37+2764delinsGTT
ENST00000278612.8:c.37+2762_37+2764delinsGTT	ENSP00000278612.8:n.37+2762_37+2764delinsGTT
ENST00000531384.1:c.37+2762_37+2764delinsGTT	ENSP00000433497.1:n.37+2762_37+2764delinsGTT
ENST00000610253.5:n.137+2762_137+2764delinsGTT
NM_002519.2:c.37+2762_37+2764delinsGTT	NP_002510.2:n.37+2762_37+2764delinsGTT
XM_011542854.1:c.37+2762_37+2764delinsGTT	XP_011541156.1:n.37+2762_37+2764delinsGTT
XM_011542855.1:c.37+2762_37+2764delinsGTT	XP_011541157.1:n.37+2762_37+2764delinsGTT
NM_001321307.1:c.37+2762_37+2764delinsGTT	NP_001308236.1:n.37+2762_37+2764delinsGTT
XM_011542854.2:c.37+2762_37+2764delinsGTT	XP_011541156.1:n.37+2762_37+2764delinsGTT
NM_002519.3:c.37+2762_37+2764delinsGTT MANE Select	NP_002510.2:n.37+2762_37+2764delinsGTT