Canonical Allele Identifier: CA1998755436

Gene: NPAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108219728_108219735delinsAAACAAAC , CM000673.2:g.108219728_108219735delinsAAACAAAC	GRCh38
NC_000011.9:g.108090455_108090462delinsAAACAAAC , CM000673.1:g.108090455_108090462delinsAAACAAAC	GRCh37
NC_000011.8:g.107595665_107595672delinsAAACAAAC	NCBI36
NG_009830.1:g.1897_1904delinsAAACAAAC , LRG_135:g.1897_1904delinsAAACAAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278612.9:c.37+2765_37+2772delinsGTTTGTTT MANE Select	ENSP00000278612.8:n.37+2765_37+2772delinsGTTTGTTT
ENST00000278612.8:c.37+2765_37+2772delinsGTTTGTTT	ENSP00000278612.8:n.37+2765_37+2772delinsGTTTGTTT
ENST00000531384.1:c.37+2765_37+2772delinsGTTTGTTT	ENSP00000433497.1:n.37+2765_37+2772delinsGTTTGTTT
ENST00000610253.5:n.137+2765_137+2772delinsGTTTGTTT
NM_002519.2:c.37+2765_37+2772delinsGTTTGTTT	NP_002510.2:n.37+2765_37+2772delinsGTTTGTTT
XM_011542854.1:c.37+2765_37+2772delinsGTTTGTTT	XP_011541156.1:n.37+2765_37+2772delinsGTTTGTTT
XM_011542855.1:c.37+2765_37+2772delinsGTTTGTTT	XP_011541157.1:n.37+2765_37+2772delinsGTTTGTTT
NM_001321307.1:c.37+2765_37+2772delinsGTTTGTTT	NP_001308236.1:n.37+2765_37+2772delinsGTTTGTTT
XM_011542854.2:c.37+2765_37+2772delinsGTTTGTTT	XP_011541156.1:n.37+2765_37+2772delinsGTTTGTTT
NM_002519.3:c.37+2765_37+2772delinsGTTTGTTT MANE Select	NP_002510.2:n.37+2765_37+2772delinsGTTTGTTT