Canonical Allele Identifier: CA1998755476
Gene: NPAT HGNC NCBI

Linked Data

dbSNP Id: rs2078467004
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108219792A>G , CM000673.2:g.108219792A>G GRCh38
NC_000011.9:g.108090519A>G , CM000673.1:g.108090519A>G GRCh37
NC_000011.8:g.107595729A>G NCBI36
NG_009830.1:g.1961A>G , LRG_135:g.1961A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000278612.9:c.37+2708T>C MANE Select ENSP00000278612.8:n.37+2708T>C
ENST00000278612.8:c.37+2708T>C ENSP00000278612.8:n.37+2708T>C
ENST00000531384.1:c.37+2708T>C ENSP00000433497.1:n.37+2708T>C
ENST00000610253.5:n.137+2708T>C
NM_002519.2:c.37+2708T>C NP_002510.2:n.37+2708T>C
XM_011542854.1:c.37+2708T>C XP_011541156.1:n.37+2708T>C
XM_011542855.1:c.37+2708T>C XP_011541157.1:n.37+2708T>C
NM_001321307.1:c.37+2708T>C NP_001308236.1:n.37+2708T>C
XM_011542854.2:c.37+2708T>C XP_011541156.1:n.37+2708T>C
NM_002519.3:c.37+2708T>C MANE Select NP_002510.2:n.37+2708T>C
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