Canonical Allele Identifier: CA671405992

Gene: NPAT

Linked Data

• dbSNP Id: rs1272324662
• MyVariant Identifiers: chr11:g.108090477del (hg19) ; chr11:g.108219750del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108219750del , CM000673.2:g.108219750del	GRCh38
NC_000011.9:g.108090477del , CM000673.1:g.108090477del	GRCh37
NC_000011.8:g.107595687del	NCBI36
NG_009830.1:g.1919del , LRG_135:g.1919del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278612.9:c.37+2750del MANE Select	ENSP00000278612.8:n.37+2750del
ENST00000278612.8:c.37+2750del	ENSP00000278612.8:n.37+2750del
ENST00000531384.1:c.37+2750del	ENSP00000433497.1:n.37+2750del
ENST00000610253.5:n.137+2750del
NM_002519.2:c.37+2750del	NP_002510.2:n.37+2750del
XM_011542854.1:c.37+2750del	XP_011541156.1:n.37+2750del
XM_011542855.1:c.37+2750del	XP_011541157.1:n.37+2750del
NM_001321307.1:c.37+2750del	NP_001308236.1:n.37+2750del
XM_011542854.2:c.37+2750del	XP_011541156.1:n.37+2750del
NM_002519.3:c.37+2750del MANE Select	NP_002510.2:n.37+2750del