Canonical Allele Identifier: CA1998755627

Gene: NPAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108220122T= , CM000673.2:g.108220122T=	GRCh38
NC_000011.9:g.108090849T= , CM000673.1:g.108090849T=	GRCh37
NC_000011.8:g.107596059T=	NCBI36
NG_009830.1:g.2291T= , LRG_135:g.2291T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278612.9:c.37+2378A= MANE Select	ENSP00000278612.8:n.37+2378A=
ENST00000278612.8:c.37+2378A=	ENSP00000278612.8:n.37+2378A=
ENST00000531384.1:c.37+2378A=	ENSP00000433497.1:n.37+2378A=
ENST00000610253.5:n.137+2378A=
NM_002519.2:c.37+2378A=	NP_002510.2:n.37+2378A=
XM_011542854.1:c.37+2378A=	XP_011541156.1:n.37+2378A=
XM_011542855.1:c.37+2378A=	XP_011541157.1:n.37+2378A=
NM_001321307.1:c.37+2378A=	NP_001308236.1:n.37+2378A=
XM_011542854.2:c.37+2378A=	XP_011541156.1:n.37+2378A=
NM_002519.3:c.37+2378A= MANE Select	NP_002510.2:n.37+2378A=