Canonical Allele Identifier: CA2278608356

Gene: NPLOC4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81629644_81629645delinsAG , CM000679.2:g.81629644_81629645delinsAG	GRCh38
NC_000017.10:g.79596670_79596671delinsAG , CM000679.1:g.79596670_79596671delinsAG	GRCh37
NC_000017.9:g.77207075_77207076delinsAG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000705719.1:c.225+80_225+81delinsCT	ENSP00000516165.1:n.225+80_225+81delinsCT...
ENST00000331134.11:c.96+80_96+81delinsCT MANE Select	ENSP00000331487.5:n.96+80_96+81delinsCT
ENST00000331134.10:c.96+80_96+81delinsCT	ENSP00000331487.5:n.96+80_96+81delinsCT
ENST00000374747.9:c.96+80_96+81delinsCT	ENSP00000363879.5:n.96+80_96+81delinsCT
ENST00000570300.1:n.117+80_117+81delinsCT
ENST00000574897.5:c.96+80_96+81delinsCT	ENSP00000461543.1:n.96+80_96+81delinsCT
ENST00000625705.1:c.93+80_93+81delinsCT	ENSP00000486640.1:n.93+80_93+81delinsCT
NM_017921.3:c.96+80_96+81delinsCT	NP_060391.2:n.96+80_96+81delinsCT
XM_011524979.1:c.96+80_96+81delinsCT	XP_011523281.1:n.96+80_96+81delinsCT
XM_011524980.1:c.96+80_96+81delinsCT	XP_011523282.1:n.96+80_96+81delinsCT
XM_011524981.1:c.96+80_96+81delinsCT	XP_011523283.1:n.96+80_96+81delinsCT
XM_011524982.1:c.96+80_96+81delinsCT	XP_011523284.1:n.96+80_96+81delinsCT
XR_934501.1:n.314+80_314+81delinsCT
XR_934502.1:n.314+80_314+81delinsCT
XM_011524982.2:c.96+80_96+81delinsCT	XP_011523284.1:n.96+80_96+81delinsCT
XR_001752557.1:n.314+80_314+81delinsCT
NM_017921.4:c.96+80_96+81delinsCT MANE Select	NP_060391.2:n.96+80_96+81delinsCT
NM_001369698.1:c.96+80_96+81delinsCT	NP_001356627.1:n.96+80_96+81delinsCT