Canonical Allele Identifier: CA942013694

Gene: NPAT

Linked Data

• dbSNP Id: rs2078470321
• gnomAD v3: 11-108220196-G-GT
• gnomAD v4: 11-108220196-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108220197dup , CM000673.2:g.108220197dup	GRCh38
NC_000011.9:g.108090924dup , CM000673.1:g.108090924dup	GRCh37
NC_000011.8:g.107596134dup	NCBI36
NG_009830.1:g.2366dup , LRG_135:g.2366dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278612.9:c.37+2303dup MANE Select	ENSP00000278612.8:n.37+2303dup
ENST00000278612.8:c.37+2303dup	ENSP00000278612.8:n.37+2303dup
ENST00000531384.1:c.37+2303dup	ENSP00000433497.1:n.37+2303dup
ENST00000610253.5:n.137+2303dup
NM_002519.2:c.37+2303dup	NP_002510.2:n.37+2303dup
XM_011542854.1:c.37+2303dup	XP_011541156.1:n.37+2303dup
XM_011542855.1:c.37+2303dup	XP_011541157.1:n.37+2303dup
NM_001321307.1:c.37+2303dup	NP_001308236.1:n.37+2303dup
XM_011542854.2:c.37+2303dup	XP_011541156.1:n.37+2303dup
NM_002519.3:c.37+2303dup MANE Select	NP_002510.2:n.37+2303dup