Canonical Allele Identifier: CA1998755626

Gene: NPAT

Linked Data

• dbSNP Id: rs2078469767

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108220124_108220127del , CM000673.2:g.108220124_108220127del	GRCh38
NC_000011.9:g.108090851_108090854del , CM000673.1:g.108090851_108090854del	GRCh37
NC_000011.8:g.107596061_107596064del	NCBI36
NG_009830.1:g.2293_2296del , LRG_135:g.2293_2296del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278612.9:c.37+2377_37+2380del MANE Select	ENSP00000278612.8:n.37+2377_37+2380del
ENST00000278612.8:c.37+2377_37+2380del	ENSP00000278612.8:n.37+2377_37+2380del
ENST00000531384.1:c.37+2377_37+2380del	ENSP00000433497.1:n.37+2377_37+2380del
ENST00000610253.5:n.137+2377_137+2380del
NM_002519.2:c.37+2377_37+2380del	NP_002510.2:n.37+2377_37+2380del
XM_011542854.1:c.37+2377_37+2380del	XP_011541156.1:n.37+2377_37+2380del
XM_011542855.1:c.37+2377_37+2380del	XP_011541157.1:n.37+2377_37+2380del
NM_001321307.1:c.37+2377_37+2380del	NP_001308236.1:n.37+2377_37+2380del
XM_011542854.2:c.37+2377_37+2380del	XP_011541156.1:n.37+2377_37+2380del
NM_002519.3:c.37+2377_37+2380del MANE Select	NP_002510.2:n.37+2377_37+2380del