Canonical Allele Identifier: CA1998755641

Gene: NPAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108220149C= , CM000673.2:g.108220149C=	GRCh38
NC_000011.9:g.108090876C= , CM000673.1:g.108090876C=	GRCh37
NC_000011.8:g.107596086C=	NCBI36
NG_009830.1:g.2318C= , LRG_135:g.2318C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278612.9:c.37+2351G= MANE Select	ENSP00000278612.8:n.37+2351G=
ENST00000278612.8:c.37+2351G=	ENSP00000278612.8:n.37+2351G=
ENST00000531384.1:c.37+2351G=	ENSP00000433497.1:n.37+2351G=
ENST00000610253.5:n.137+2351G=
NM_002519.2:c.37+2351G=	NP_002510.2:n.37+2351G=
XM_011542854.1:c.37+2351G=	XP_011541156.1:n.37+2351G=
XM_011542855.1:c.37+2351G=	XP_011541157.1:n.37+2351G=
NM_001321307.1:c.37+2351G=	NP_001308236.1:n.37+2351G=
XM_011542854.2:c.37+2351G=	XP_011541156.1:n.37+2351G=
NM_002519.3:c.37+2351G= MANE Select	NP_002510.2:n.37+2351G=