Canonical Allele Identifier: CA2278608393

Gene: NPLOC4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81629712A= , CM000679.2:g.81629712A=	GRCh38
NC_000017.10:g.79596738A= , CM000679.1:g.79596738A=	GRCh37
NC_000017.9:g.77207143A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000705719.1:c.225+13T=	ENSP00000516165.1:n.225+13T=
ENST00000331134.11:c.96+13T= MANE Select	ENSP00000331487.5:n.96+13T=
ENST00000331134.10:c.96+13T=	ENSP00000331487.5:n.96+13T=
ENST00000374747.9:c.96+13T=	ENSP00000363879.5:n.96+13T=
ENST00000570300.1:n.117+13T=
ENST00000574897.5:c.96+13T=	ENSP00000461543.1:n.96+13T=
ENST00000625705.1:c.93+13T=	ENSP00000486640.1:n.93+13T=
NM_017921.3:c.96+13T=	NP_060391.2:n.96+13T=
XM_011524979.1:c.96+13T=	XP_011523281.1:n.96+13T=
XM_011524980.1:c.96+13T=	XP_011523282.1:n.96+13T=
XM_011524981.1:c.96+13T=	XP_011523283.1:n.96+13T=
XM_011524982.1:c.96+13T=	XP_011523284.1:n.96+13T=
XR_934501.1:n.314+13T=
XR_934502.1:n.314+13T=
XM_011524982.2:c.96+13T=	XP_011523284.1:n.96+13T=
XR_001752557.1:n.314+13T=
NM_017921.4:c.96+13T= MANE Select	NP_060391.2:n.96+13T=
NM_001369698.1:c.96+13T=	NP_001356627.1:n.96+13T=