Canonical Allele Identifier: CA2278608411

Gene: NPLOC4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81629771C= , CM000679.2:g.81629771C=	GRCh38
NC_000017.10:g.79596797C= , CM000679.1:g.79596797C=	GRCh37
NC_000017.9:g.77207202C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000705719.1:c.179G=	ENSP00000516165.1:p.Arg60=
ENST00000331134.11:c.50G= MANE Select	ENSP00000331487.5:p.Arg17=
ENST00000331134.10:c.50G=	ENSP00000331487.5:p.Arg17=
ENST00000374747.9:c.50G=	ENSP00000363879.5:p.Arg17=
ENST00000570300.1:n.71G=
ENST00000574897.5:c.50G=	ENSP00000461543.1:p.Arg17=
ENST00000625705.1:c.47G=	ENSP00000486640.1:p.Arg16=
NM_017921.3:c.50G=	NP_060391.2:p.Arg17=
XM_011524979.1:c.50G=	XP_011523281.1:p.Arg17=
XM_011524980.1:c.50G=	XP_011523282.1:p.Arg17=
XM_011524981.1:c.50G=	XP_011523283.1:p.Arg17=
XM_011524982.1:c.50G=	XP_011523284.1:p.Arg17=
XR_934501.1:n.268G=
XR_934502.1:n.268G=
XM_011524982.2:c.50G=	XP_011523284.1:p.Arg17=
XR_001752557.1:n.268G=
NM_017921.4:c.50G= MANE Select	NP_060391.2:p.Arg17=
NM_001369698.1:c.50G=	NP_001356627.1:p.Arg17=