Canonical Allele Identifier: CA401463404

Gene: NPLOC4

Linked Data

• COSMIC: COSM3748654 ; COSM3748655
• MyVariant Identifiers: chr17:g.79596767G>A (hg19) ; chr17:g.81629741G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81629741G>A , CM000679.2:g.81629741G>A	GRCh38
NC_000017.10:g.79596767G>A , CM000679.1:g.79596767G>A	GRCh37
NC_000017.9:g.77207172G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000705719.1:c.209C>T	ENSP00000516165.1:p.Ala70Val
ENST00000331134.11:c.80C>T MANE Select	ENSP00000331487.5:p.Ala27Val
ENST00000331134.10:c.80C>T	ENSP00000331487.5:p.Ala27Val
ENST00000374747.9:c.80C>T	ENSP00000363879.5:p.Ala27Val
ENST00000570300.1:n.101C>T
ENST00000574897.5:c.80C>T	ENSP00000461543.1:p.Ala27Val
ENST00000625705.1:c.77C>T	ENSP00000486640.1:p.Ala26Val
NM_017921.3:c.80C>T	NP_060391.2:p.Ala27Val
XM_011524979.1:c.80C>T	XP_011523281.1:p.Ala27Val
XM_011524980.1:c.80C>T	XP_011523282.1:p.Ala27Val
XM_011524981.1:c.80C>T	XP_011523283.1:p.Ala27Val
XM_011524982.1:c.80C>T	XP_011523284.1:p.Ala27Val
XR_934501.1:n.298C>T
XR_934502.1:n.298C>T
XM_011524982.2:c.80C>T	XP_011523284.1:p.Ala27Val
XR_001752557.1:n.298C>T
NM_017921.4:c.80C>T MANE Select	NP_060391.2:p.Ala27Val
NM_001369698.1:c.80C>T	NP_001356627.1:p.Ala27Val