Canonical Allele Identifier: CA401463543

Gene: NPLOC4

Linked Data

• MyVariant Identifiers: chr17:g.79596808A>T (hg19) ; chr17:g.81629782A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81629782A>T , CM000679.2:g.81629782A>T	GRCh38
NC_000017.10:g.79596808A>T , CM000679.1:g.79596808A>T	GRCh37
NC_000017.9:g.77207213A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000705719.1:c.168T>A	ENSP00000516165.1:p.Asp56Glu
ENST00000331134.11:c.39T>A MANE Select	ENSP00000331487.5:p.Asp13Glu
ENST00000331134.10:c.39T>A	ENSP00000331487.5:p.Asp13Glu
ENST00000374747.9:c.39T>A	ENSP00000363879.5:p.Asp13Glu
ENST00000570300.1:n.60T>A
ENST00000574897.5:c.39T>A	ENSP00000461543.1:p.Asp13Glu
ENST00000625705.1:c.36T>A	ENSP00000486640.1:p.Asp12Glu
NM_017921.3:c.39T>A	NP_060391.2:p.Asp13Glu
XM_011524979.1:c.39T>A	XP_011523281.1:p.Asp13Glu
XM_011524980.1:c.39T>A	XP_011523282.1:p.Asp13Glu
XM_011524981.1:c.39T>A	XP_011523283.1:p.Asp13Glu
XM_011524982.1:c.39T>A	XP_011523284.1:p.Asp13Glu
XR_934501.1:n.257T>A
XR_934502.1:n.257T>A
XM_011524982.2:c.39T>A	XP_011523284.1:p.Asp13Glu
XR_001752557.1:n.257T>A
NM_017921.4:c.39T>A MANE Select	NP_060391.2:p.Asp13Glu
NM_001369698.1:c.39T>A	NP_001356627.1:p.Asp13Glu