Canonical Allele Identifier: CA2278608414

Gene: NPLOC4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81629778C= , CM000679.2:g.81629778C=	GRCh38
NC_000017.10:g.79596804C= , CM000679.1:g.79596804C=	GRCh37
NC_000017.9:g.77207209C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000705719.1:c.172G=	ENSP00000516165.1:p.Val58=
ENST00000331134.11:c.43G= MANE Select	ENSP00000331487.5:p.Val15=
ENST00000331134.10:c.43G=	ENSP00000331487.5:p.Val15=
ENST00000374747.9:c.43G=	ENSP00000363879.5:p.Val15=
ENST00000570300.1:n.64G=
ENST00000574897.5:c.43G=	ENSP00000461543.1:p.Val15=
ENST00000625705.1:c.40G=	ENSP00000486640.1:p.Val14=
NM_017921.3:c.43G=	NP_060391.2:p.Val15=
XM_011524979.1:c.43G=	XP_011523281.1:p.Val15=
XM_011524980.1:c.43G=	XP_011523282.1:p.Val15=
XM_011524981.1:c.43G=	XP_011523283.1:p.Val15=
XM_011524982.1:c.43G=	XP_011523284.1:p.Val15=
XR_934501.1:n.261G=
XR_934502.1:n.261G=
XM_011524982.2:c.43G=	XP_011523284.1:p.Val15=
XR_001752557.1:n.261G=
NM_017921.4:c.43G= MANE Select	NP_060391.2:p.Val15=
NM_001369698.1:c.43G=	NP_001356627.1:p.Val15=