Canonical Allele Identifier: CA2793552006
Gene: NPAT HGNC NCBI

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