Canonical Allele Identifier: CA1998755658

Gene: NPAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108220185_108220188delinsCACA , CM000673.2:g.108220185_108220188delinsCACA	GRCh38
NC_000011.9:g.108090912_108090915delinsCACA , CM000673.1:g.108090912_108090915delinsCACA	GRCh37
NC_000011.8:g.107596122_107596125delinsCACA	NCBI36
NG_009830.1:g.2354_2357delinsCACA , LRG_135:g.2354_2357delinsCACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278612.9:c.37+2312_37+2315delinsTGTG MANE Select	ENSP00000278612.8:n.37+2312_37+2315delinsTGTG
ENST00000278612.8:c.37+2312_37+2315delinsTGTG	ENSP00000278612.8:n.37+2312_37+2315delinsTGTG
ENST00000531384.1:c.37+2312_37+2315delinsTGTG	ENSP00000433497.1:n.37+2312_37+2315delinsTGTG
ENST00000610253.5:n.137+2312_137+2315delinsTGTG
NM_002519.2:c.37+2312_37+2315delinsTGTG	NP_002510.2:n.37+2312_37+2315delinsTGTG
XM_011542854.1:c.37+2312_37+2315delinsTGTG	XP_011541156.1:n.37+2312_37+2315delinsTGTG
XM_011542855.1:c.37+2312_37+2315delinsTGTG	XP_011541157.1:n.37+2312_37+2315delinsTGTG
NM_001321307.1:c.37+2312_37+2315delinsTGTG	NP_001308236.1:n.37+2312_37+2315delinsTGTG
XM_011542854.2:c.37+2312_37+2315delinsTGTG	XP_011541156.1:n.37+2312_37+2315delinsTGTG
NM_002519.3:c.37+2312_37+2315delinsTGTG MANE Select	NP_002510.2:n.37+2312_37+2315delinsTGTG