Canonical Allele Identifier: CA1998755660

Gene: NPAT

Linked Data

• dbSNP Id: rs2078470245

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108220189_108220191del , CM000673.2:g.108220189_108220191del	GRCh38
NC_000011.9:g.108090916_108090918del , CM000673.1:g.108090916_108090918del	GRCh37
NC_000011.8:g.107596126_107596128del	NCBI36
NG_009830.1:g.2358_2360del , LRG_135:g.2358_2360del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278612.9:c.37+2312_37+2314del MANE Select	ENSP00000278612.8:n.37+2312_37+2314del
ENST00000278612.8:c.37+2312_37+2314del	ENSP00000278612.8:n.37+2312_37+2314del
ENST00000531384.1:c.37+2312_37+2314del	ENSP00000433497.1:n.37+2312_37+2314del
ENST00000610253.5:n.137+2312_137+2314del
NM_002519.2:c.37+2312_37+2314del	NP_002510.2:n.37+2312_37+2314del
XM_011542854.1:c.37+2312_37+2314del	XP_011541156.1:n.37+2312_37+2314del
XM_011542855.1:c.37+2312_37+2314del	XP_011541157.1:n.37+2312_37+2314del
NM_001321307.1:c.37+2312_37+2314del	NP_001308236.1:n.37+2312_37+2314del
XM_011542854.2:c.37+2312_37+2314del	XP_011541156.1:n.37+2312_37+2314del
NM_002519.3:c.37+2312_37+2314del MANE Select	NP_002510.2:n.37+2312_37+2314del