Canonical Allele Identifier: CA401463427

Gene: NPLOC4

Linked Data

• dbSNP Id: rs1373359695
• MyVariant Identifiers: chr17:g.79596775T>A (hg19) ; chr17:g.81629749T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81629749T>A , CM000679.2:g.81629749T>A	GRCh38
NC_000017.10:g.79596775T>A , CM000679.1:g.79596775T>A	GRCh37
NC_000017.9:g.77207180T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000705719.1:c.201A>T	ENSP00000516165.1:p.Glu67Asp
ENST00000331134.11:c.72A>T MANE Select	ENSP00000331487.5:p.Glu24Asp
ENST00000331134.10:c.72A>T	ENSP00000331487.5:p.Glu24Asp
ENST00000374747.9:c.72A>T	ENSP00000363879.5:p.Glu24Asp
ENST00000570300.1:n.93A>T
ENST00000574897.5:c.72A>T	ENSP00000461543.1:p.Glu24Asp
ENST00000625705.1:c.69A>T	ENSP00000486640.1:p.Glu23Asp
NM_017921.3:c.72A>T	NP_060391.2:p.Glu24Asp
XM_011524979.1:c.72A>T	XP_011523281.1:p.Glu24Asp
XM_011524980.1:c.72A>T	XP_011523282.1:p.Glu24Asp
XM_011524981.1:c.72A>T	XP_011523283.1:p.Glu24Asp
XM_011524982.1:c.72A>T	XP_011523284.1:p.Glu24Asp
XR_934501.1:n.290A>T
XR_934502.1:n.290A>T
XM_011524982.2:c.72A>T	XP_011523284.1:p.Glu24Asp
XR_001752557.1:n.290A>T
NM_017921.4:c.72A>T MANE Select	NP_060391.2:p.Glu24Asp
NM_001369698.1:c.72A>T	NP_001356627.1:p.Glu24Asp