Canonical Allele Identifier: CA2278608477
Gene: NPLOC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81629896_81629905delinsGGTCACTGAA , CM000679.2:g.81629896_81629905delinsGGTCACTGAA GRCh38
NC_000017.10:g.79596922_79596931delinsGGTCACTGAA , CM000679.1:g.79596922_79596931delinsGGTCACTGAA GRCh37
NC_000017.9:g.77207327_77207336delinsGGTCACTGAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000705719.1:c.145-100_145-91delinsTTCAGTGACC ENSP00000516165.1:n.145-100_145-91delinsTTCAGTGACC
ENST00000331134.11:c.16-100_16-91delinsTTCAGTGACC MANE Select ENSP00000331487.5:n.16-100_16-91delinsTTCAGTGACC
ENST00000331134.10:c.16-100_16-91delinsTTCAGTGACC ENSP00000331487.5:n.16-100_16-91delinsTTCAGTGACC
ENST00000374747.9:c.16-100_16-91delinsTTCAGTGACC ENSP00000363879.5:n.16-100_16-91delinsTTCAGTGACC
ENST00000570300.1:n.37-100_37-91delinsTTCAGTGACC
ENST00000574897.5:c.16-100_16-91delinsTTCAGTGACC ENSP00000461543.1:n.16-100_16-91delinsTTCAGTGACC
NM_017921.3:c.16-100_16-91delinsTTCAGTGACC NP_060391.2:n.16-100_16-91delinsTTCAGTGACC
XM_011524979.1:c.16-100_16-91delinsTTCAGTGACC XP_011523281.1:n.16-100_16-91delinsTTCAGTGACC
XM_011524980.1:c.16-100_16-91delinsTTCAGTGACC XP_011523282.1:n.16-100_16-91delinsTTCAGTGACC
XM_011524981.1:c.16-100_16-91delinsTTCAGTGACC XP_011523283.1:n.16-100_16-91delinsTTCAGTGACC
XM_011524982.1:c.16-100_16-91delinsTTCAGTGACC XP_011523284.1:n.16-100_16-91delinsTTCAGTGACC
XR_934501.1:n.234-100_234-91delinsTTCAGTGACC
XR_934502.1:n.234-100_234-91delinsTTCAGTGACC
XM_011524982.2:c.16-100_16-91delinsTTCAGTGACC XP_011523284.1:n.16-100_16-91delinsTTCAGTGACC
XR_001752557.1:n.234-100_234-91delinsTTCAGTGACC
NM_017921.4:c.16-100_16-91delinsTTCAGTGACC MANE Select NP_060391.2:n.16-100_16-91delinsTTCAGTGACC
NM_001369698.1:c.16-100_16-91delinsTTCAGTGACC NP_001356627.1:n.16-100_16-91delinsTTCAGTGACC