Canonical Allele Identifier: CA2793552006

Gene: NPAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108220040T>C , CM000673.2:g.108220040T>C	GRCh38
NC_000011.9:g.108090767T>C , CM000673.1:g.108090767T>C	GRCh37
NC_000011.8:g.107595977T>C	NCBI36
NG_009830.1:g.2209T>C , LRG_135:g.2209T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000278612.9:c.37+2460A>G MANE Select	ENSP00000278612.8:n.37+2460A>G
ENST00000278612.8:c.37+2460A>G	ENSP00000278612.8:n.37+2460A>G
ENST00000531384.1:c.37+2460A>G	ENSP00000433497.1:n.37+2460A>G
ENST00000610253.5:n.137+2460A>G
NM_002519.2:c.37+2460A>G	NP_002510.2:n.37+2460A>G
XM_011542854.1:c.37+2460A>G	XP_011541156.1:n.37+2460A>G
XM_011542855.1:c.37+2460A>G	XP_011541157.1:n.37+2460A>G
NM_001321307.1:c.37+2460A>G	NP_001308236.1:n.37+2460A>G
XM_011542854.2:c.37+2460A>G	XP_011541156.1:n.37+2460A>G
NM_002519.3:c.37+2460A>G MANE Select	NP_002510.2:n.37+2460A>G