Canonical Allele Identifier: CA228361743
Gene: NPAT HGNC NCBI

Linked Data

dbSNP Id: rs901495102

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108220039A>G , CM000673.2:g.108220039A>G GRCh38
NC_000011.9:g.108090766A>G , CM000673.1:g.108090766A>G GRCh37
NC_000011.8:g.107595976A>G NCBI36
NG_009830.1:g.2208A>G , LRG_135:g.2208A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000278612.9:c.37+2461T>C MANE Select ENSP00000278612.8:n.37+2461T>C
ENST00000278612.8:c.37+2461T>C ENSP00000278612.8:n.37+2461T>C
ENST00000531384.1:c.37+2461T>C ENSP00000433497.1:n.37+2461T>C
ENST00000610253.5:n.137+2461T>C
NM_002519.2:c.37+2461T>C NP_002510.2:n.37+2461T>C
XM_011542854.1:c.37+2461T>C XP_011541156.1:n.37+2461T>C
XM_011542855.1:c.37+2461T>C XP_011541157.1:n.37+2461T>C
NM_001321307.1:c.37+2461T>C NP_001308236.1:n.37+2461T>C
XM_011542854.2:c.37+2461T>C XP_011541156.1:n.37+2461T>C
NM_002519.3:c.37+2461T>C MANE Select NP_002510.2:n.37+2461T>C