Canonical Allele Identifier: CA1998755447

Gene: NPAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108219739A= , CM000673.2:g.108219739A=	GRCh38
NC_000011.9:g.108090466A= , CM000673.1:g.108090466A=	GRCh37
NC_000011.8:g.107595676A=	NCBI36
NG_009830.1:g.1908A= , LRG_135:g.1908A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278612.9:c.37+2761T= MANE Select	ENSP00000278612.8:n.37+2761T=
ENST00000278612.8:c.37+2761T=	ENSP00000278612.8:n.37+2761T=
ENST00000531384.1:c.37+2761T=	ENSP00000433497.1:n.37+2761T=
ENST00000610253.5:n.137+2761T=
NM_002519.2:c.37+2761T=	NP_002510.2:n.37+2761T=
XM_011542854.1:c.37+2761T=	XP_011541156.1:n.37+2761T=
XM_011542855.1:c.37+2761T=	XP_011541157.1:n.37+2761T=
NM_001321307.1:c.37+2761T=	NP_001308236.1:n.37+2761T=
XM_011542854.2:c.37+2761T=	XP_011541156.1:n.37+2761T=
NM_002519.3:c.37+2761T= MANE Select	NP_002510.2:n.37+2761T=