Canonical Allele Identifier: CA1998755550

Gene: NPAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108219961_108219966delinsTGAATA , CM000673.2:g.108219961_108219966delinsTGAATA	GRCh38
NC_000011.9:g.108090688_108090693delinsTGAATA , CM000673.1:g.108090688_108090693delinsTGAATA	GRCh37
NC_000011.8:g.107595898_107595903delinsTGAATA	NCBI36
NG_009830.1:g.2130_2135delinsTGAATA , LRG_135:g.2130_2135delinsTGAATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278612.9:c.37+2534_37+2539delinsTATTCA MANE Select	ENSP00000278612.8:n.37+2534_37+2539delinsTATTCA
ENST00000278612.8:c.37+2534_37+2539delinsTATTCA	ENSP00000278612.8:n.37+2534_37+2539delinsTATTCA
ENST00000531384.1:c.37+2534_37+2539delinsTATTCA	ENSP00000433497.1:n.37+2534_37+2539delinsTATTCA
ENST00000610253.5:n.137+2534_137+2539delinsTATTCA
NM_002519.2:c.37+2534_37+2539delinsTATTCA	NP_002510.2:n.37+2534_37+2539delinsTATTCA
XM_011542854.1:c.37+2534_37+2539delinsTATTCA	XP_011541156.1:n.37+2534_37+2539delinsTATTCA
XM_011542855.1:c.37+2534_37+2539delinsTATTCA	XP_011541157.1:n.37+2534_37+2539delinsTATTCA
NM_001321307.1:c.37+2534_37+2539delinsTATTCA	NP_001308236.1:n.37+2534_37+2539delinsTATTCA
XM_011542854.2:c.37+2534_37+2539delinsTATTCA	XP_011541156.1:n.37+2534_37+2539delinsTATTCA
NM_002519.3:c.37+2534_37+2539delinsTATTCA MANE Select	NP_002510.2:n.37+2534_37+2539delinsTATTCA