Canonical Allele Identifier: CA2278608427
Gene: NPLOC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81629809T= , CM000679.2:g.81629809T= GRCh38
NC_000017.10:g.79596835T= , CM000679.1:g.79596835T= GRCh37
NC_000017.9:g.77207240T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000705719.1:c.145-4A= ENSP00000516165.1:n.145-4A=
ENST00000331134.11:c.16-4A= MANE Select ENSP00000331487.5:n.16-4A=
ENST00000331134.10:c.16-4A= ENSP00000331487.5:n.16-4A=
ENST00000374747.9:c.16-4A= ENSP00000363879.5:n.16-4A=
ENST00000570300.1:n.37-4A=
ENST00000574897.5:c.16-4A= ENSP00000461543.1:n.16-4A=
ENST00000625705.1:c.13-4A= ENSP00000486640.1:n.13-4A=
NM_017921.3:c.16-4A= NP_060391.2:n.16-4A=
XM_011524979.1:c.16-4A= XP_011523281.1:n.16-4A=
XM_011524980.1:c.16-4A= XP_011523282.1:n.16-4A=
XM_011524981.1:c.16-4A= XP_011523283.1:n.16-4A=
XM_011524982.1:c.16-4A= XP_011523284.1:n.16-4A=
XR_934501.1:n.234-4A=
XR_934502.1:n.234-4A=
XM_011524982.2:c.16-4A= XP_011523284.1:n.16-4A=
XR_001752557.1:n.234-4A=
NM_017921.4:c.16-4A= MANE Select NP_060391.2:n.16-4A=
NM_001369698.1:c.16-4A= NP_001356627.1:n.16-4A=