Canonical Allele Identifier: CA2725091895

Gene: NPAT

Linked Data

• dbSNP Id: rs2134910465

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108220012T>A , CM000673.2:g.108220012T>A	GRCh38
NC_000011.9:g.108090739T>A , CM000673.1:g.108090739T>A	GRCh37
NC_000011.8:g.107595949T>A	NCBI36
NG_009830.1:g.2181T>A , LRG_135:g.2181T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278612.9:c.37+2488A>T MANE Select	ENSP00000278612.8:n.37+2488A>T
ENST00000278612.8:c.37+2488A>T	ENSP00000278612.8:n.37+2488A>T
ENST00000531384.1:c.37+2488A>T	ENSP00000433497.1:n.37+2488A>T
ENST00000610253.5:n.137+2488A>T
NM_002519.2:c.37+2488A>T	NP_002510.2:n.37+2488A>T
XM_011542854.1:c.37+2488A>T	XP_011541156.1:n.37+2488A>T
XM_011542855.1:c.37+2488A>T	XP_011541157.1:n.37+2488A>T
NM_001321307.1:c.37+2488A>T	NP_001308236.1:n.37+2488A>T
XM_011542854.2:c.37+2488A>T	XP_011541156.1:n.37+2488A>T
NM_002519.3:c.37+2488A>T MANE Select	NP_002510.2:n.37+2488A>T