Canonical Allele Identifier: CA1998755625

Gene: NPAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108220119_108220123delinsGAATA , CM000673.2:g.108220119_108220123delinsGAATA	GRCh38
NC_000011.9:g.108090846_108090850delinsGAATA , CM000673.1:g.108090846_108090850delinsGAATA	GRCh37
NC_000011.8:g.107596056_107596060delinsGAATA	NCBI36
NG_009830.1:g.2288_2292delinsGAATA , LRG_135:g.2288_2292delinsGAATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278612.9:c.37+2377_37+2381delinsTATTC MANE Select	ENSP00000278612.8:n.37+2377_37+2381delinsTATTC
ENST00000278612.8:c.37+2377_37+2381delinsTATTC	ENSP00000278612.8:n.37+2377_37+2381delinsTATTC
ENST00000531384.1:c.37+2377_37+2381delinsTATTC	ENSP00000433497.1:n.37+2377_37+2381delinsTATTC
ENST00000610253.5:n.137+2377_137+2381delinsTATTC
NM_002519.2:c.37+2377_37+2381delinsTATTC	NP_002510.2:n.37+2377_37+2381delinsTATTC
XM_011542854.1:c.37+2377_37+2381delinsTATTC	XP_011541156.1:n.37+2377_37+2381delinsTATTC
XM_011542855.1:c.37+2377_37+2381delinsTATTC	XP_011541157.1:n.37+2377_37+2381delinsTATTC
NM_001321307.1:c.37+2377_37+2381delinsTATTC	NP_001308236.1:n.37+2377_37+2381delinsTATTC
XM_011542854.2:c.37+2377_37+2381delinsTATTC	XP_011541156.1:n.37+2377_37+2381delinsTATTC
NM_002519.3:c.37+2377_37+2381delinsTATTC MANE Select	NP_002510.2:n.37+2377_37+2381delinsTATTC