Canonical Allele Identifier: CA918963568

Gene: NPAT

Linked Data

• dbSNP Id: rs869248950

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108219759_108219760dup , CM000673.2:g.108219759_108219760dup	GRCh38
NC_000011.9:g.108090486_108090487dup , CM000673.1:g.108090486_108090487dup	GRCh37
NC_000011.8:g.107595696_107595697dup	NCBI36
NG_009830.1:g.1928_1929dup , LRG_135:g.1928_1929dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278612.9:c.37+2741_37+2742dup MANE Select	ENSP00000278612.8:n.37+2741_37+2742dup
ENST00000278612.8:c.37+2741_37+2742dup	ENSP00000278612.8:n.37+2741_37+2742dup
ENST00000531384.1:c.37+2741_37+2742dup	ENSP00000433497.1:n.37+2741_37+2742dup
ENST00000610253.5:n.137+2741_137+2742dup
NM_002519.2:c.37+2741_37+2742dup	NP_002510.2:n.37+2741_37+2742dup
XM_011542854.1:c.37+2741_37+2742dup	XP_011541156.1:n.37+2741_37+2742dup
XM_011542855.1:c.37+2741_37+2742dup	XP_011541157.1:n.37+2741_37+2742dup
NM_001321307.1:c.37+2741_37+2742dup	NP_001308236.1:n.37+2741_37+2742dup
XM_011542854.2:c.37+2741_37+2742dup	XP_011541156.1:n.37+2741_37+2742dup
NM_002519.3:c.37+2741_37+2742dup MANE Select	NP_002510.2:n.37+2741_37+2742dup