Canonical Allele Identifier: CA1998755450

Gene: NPAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108219749_108219753delinsACAAC , CM000673.2:g.108219749_108219753delinsACAAC	GRCh38
NC_000011.9:g.108090476_108090480delinsACAAC , CM000673.1:g.108090476_108090480delinsACAAC	GRCh37
NC_000011.8:g.107595686_107595690delinsACAAC	NCBI36
NG_009830.1:g.1918_1922delinsACAAC , LRG_135:g.1918_1922delinsACAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278612.9:c.37+2747_37+2751delinsGTTGT MANE Select	ENSP00000278612.8:n.37+2747_37+2751delinsGTTGT
ENST00000278612.8:c.37+2747_37+2751delinsGTTGT	ENSP00000278612.8:n.37+2747_37+2751delinsGTTGT
ENST00000531384.1:c.37+2747_37+2751delinsGTTGT	ENSP00000433497.1:n.37+2747_37+2751delinsGTTGT
ENST00000610253.5:n.137+2747_137+2751delinsGTTGT
NM_002519.2:c.37+2747_37+2751delinsGTTGT	NP_002510.2:n.37+2747_37+2751delinsGTTGT
XM_011542854.1:c.37+2747_37+2751delinsGTTGT	XP_011541156.1:n.37+2747_37+2751delinsGTTGT
XM_011542855.1:c.37+2747_37+2751delinsGTTGT	XP_011541157.1:n.37+2747_37+2751delinsGTTGT
NM_001321307.1:c.37+2747_37+2751delinsGTTGT	NP_001308236.1:n.37+2747_37+2751delinsGTTGT
XM_011542854.2:c.37+2747_37+2751delinsGTTGT	XP_011541156.1:n.37+2747_37+2751delinsGTTGT
NM_002519.3:c.37+2747_37+2751delinsGTTGT MANE Select	NP_002510.2:n.37+2747_37+2751delinsGTTGT