Canonical Allele Identifier: CA1998755428

Gene: NPAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108219713T= , CM000673.2:g.108219713T=	GRCh38
NC_000011.9:g.108090440T= , CM000673.1:g.108090440T=	GRCh37
NC_000011.8:g.107595650T=	NCBI36
NG_009830.1:g.1882T= , LRG_135:g.1882T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278612.9:c.37+2787A= MANE Select	ENSP00000278612.8:n.37+2787A=
ENST00000278612.8:c.37+2787A=	ENSP00000278612.8:n.37+2787A=
ENST00000531384.1:c.37+2787A=	ENSP00000433497.1:n.37+2787A=
ENST00000610253.5:n.137+2787A=
NM_002519.2:c.37+2787A=	NP_002510.2:n.37+2787A=
XM_011542854.1:c.37+2787A=	XP_011541156.1:n.37+2787A=
XM_011542855.1:c.37+2787A=	XP_011541157.1:n.37+2787A=
NM_001321307.1:c.37+2787A=	NP_001308236.1:n.37+2787A=
XM_011542854.2:c.37+2787A=	XP_011541156.1:n.37+2787A=
NM_002519.3:c.37+2787A= MANE Select	NP_002510.2:n.37+2787A=