Canonical Allele Identifier: CA671406054

Gene: NPAT

Linked Data

• dbSNP Id: rs1341589412
• MyVariant Identifiers: chr11:g.108090787_108090788del (hg19) ; chr11:g.108220060_108220061del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108220061_108220062del , CM000673.2:g.108220061_108220062del	GRCh38
NC_000011.9:g.108090788_108090789del , CM000673.1:g.108090788_108090789del	GRCh37
NC_000011.8:g.107595998_107595999del	NCBI36
NG_009830.1:g.2230_2231del , LRG_135:g.2230_2231del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278612.9:c.37+2439_37+2440del MANE Select	ENSP00000278612.8:n.37+2439_37+2440del
ENST00000278612.8:c.37+2439_37+2440del	ENSP00000278612.8:n.37+2439_37+2440del
ENST00000531384.1:c.37+2439_37+2440del	ENSP00000433497.1:n.37+2439_37+2440del
ENST00000610253.5:n.137+2439_137+2440del
NM_002519.2:c.37+2439_37+2440del	NP_002510.2:n.37+2439_37+2440del
XM_011542854.1:c.37+2439_37+2440del	XP_011541156.1:n.37+2439_37+2440del
XM_011542855.1:c.37+2439_37+2440del	XP_011541157.1:n.37+2439_37+2440del
NM_001321307.1:c.37+2439_37+2440del	NP_001308236.1:n.37+2439_37+2440del
XM_011542854.2:c.37+2439_37+2440del	XP_011541156.1:n.37+2439_37+2440del
NM_002519.3:c.37+2439_37+2440del MANE Select	NP_002510.2:n.37+2439_37+2440del