Canonical Allele Identifier: CA2278608420

Gene: NPLOC4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81629791C= , CM000679.2:g.81629791C=	GRCh38
NC_000017.10:g.79596817C= , CM000679.1:g.79596817C=	GRCh37
NC_000017.9:g.77207222C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000705719.1:c.159G=	ENSP00000516165.1:p.Gln53=
ENST00000331134.11:c.30G= MANE Select	ENSP00000331487.5:p.Gln10=
ENST00000331134.10:c.30G=	ENSP00000331487.5:p.Gln10=
ENST00000374747.9:c.30G=	ENSP00000363879.5:p.Gln10=
ENST00000570300.1:n.51G=
ENST00000574897.5:c.30G=	ENSP00000461543.1:p.Gln10=
ENST00000625705.1:c.27G=	ENSP00000486640.1:p.Gln9=
NM_017921.3:c.30G=	NP_060391.2:p.Gln10=
XM_011524979.1:c.30G=	XP_011523281.1:p.Gln10=
XM_011524980.1:c.30G=	XP_011523282.1:p.Gln10=
XM_011524981.1:c.30G=	XP_011523283.1:p.Gln10=
XM_011524982.1:c.30G=	XP_011523284.1:p.Gln10=
XR_934501.1:n.248G=
XR_934502.1:n.248G=
XM_011524982.2:c.30G=	XP_011523284.1:p.Gln10=
XR_001752557.1:n.248G=
NM_017921.4:c.30G= MANE Select	NP_060391.2:p.Gln10=
NM_001369698.1:c.30G=	NP_001356627.1:p.Gln10=