Canonical Allele Identifier: CA2278608424
Gene: NPLOC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81629803T= , CM000679.2:g.81629803T= GRCh38
NC_000017.10:g.79596829T= , CM000679.1:g.79596829T= GRCh37
NC_000017.9:g.77207234T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000705719.1:c.147A= ENSP00000516165.1:p.Ile49=
ENST00000331134.11:c.18A= MANE Select ENSP00000331487.5:p.Ile6=
ENST00000331134.10:c.18A= ENSP00000331487.5:p.Ile6=
ENST00000374747.9:c.18A= ENSP00000363879.5:p.Ile6=
ENST00000570300.1:n.39A=
ENST00000574897.5:c.18A= ENSP00000461543.1:p.Ile6=
ENST00000625705.1:c.15A= ENSP00000486640.1:p.Ile5=
NM_017921.3:c.18A= NP_060391.2:p.Ile6=
XM_011524979.1:c.18A= XP_011523281.1:p.Ile6=
XM_011524980.1:c.18A= XP_011523282.1:p.Ile6=
XM_011524981.1:c.18A= XP_011523283.1:p.Ile6=
XM_011524982.1:c.18A= XP_011523284.1:p.Ile6=
XR_934501.1:n.236A=
XR_934502.1:n.236A=
XM_011524982.2:c.18A= XP_011523284.1:p.Ile6=
XR_001752557.1:n.236A=
NM_017921.4:c.18A= MANE Select NP_060391.2:p.Ile6=
NM_001369698.1:c.18A= NP_001356627.1:p.Ile6=