Canonical Allele Identifier: CA601692944
Gene: NPAT HGNC NCBI

Linked Data

dbSNP Id: rs1171135707
gnomAD v2: 11-108090874-G-GC
MyVariant Identifiers: chr11:g.108090874_108090875insC (hg19) chr11:g.108220147_108220148insC (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108220150dup , CM000673.2:g.108220150dup GRCh38
NC_000011.9:g.108090877dup , CM000673.1:g.108090877dup GRCh37
NC_000011.8:g.107596087dup NCBI36
NG_009830.1:g.2319dup , LRG_135:g.2319dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000278612.9:c.37+2352dup MANE Select ENSP00000278612.8:n.37+2352dup
ENST00000278612.8:c.37+2352dup ENSP00000278612.8:n.37+2352dup
ENST00000531384.1:c.37+2352dup ENSP00000433497.1:n.37+2352dup
ENST00000610253.5:n.137+2352dup
NM_002519.2:c.37+2352dup NP_002510.2:n.37+2352dup
XM_011542854.1:c.37+2352dup XP_011541156.1:n.37+2352dup
XM_011542855.1:c.37+2352dup XP_011541157.1:n.37+2352dup
NM_001321307.1:c.37+2352dup NP_001308236.1:n.37+2352dup
XM_011542854.2:c.37+2352dup XP_011541156.1:n.37+2352dup
NM_002519.3:c.37+2352dup MANE Select NP_002510.2:n.37+2352dup
Search 100 bp 5'
Search 100 bp 3'