Canonical Allele Identifier: CA401463368
Gene: NPLOC4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81629725C>G , CM000679.2:g.81629725C>G GRCh38
NC_000017.10:g.79596751C>G , CM000679.1:g.79596751C>G GRCh37
NC_000017.9:g.77207156C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000705719.1:c.225G>C ENSP00000516165.1:p.Lys75Asn
ENST00000331134.11:c.96G>C MANE Select ENSP00000331487.5:p.Lys32Asn
ENST00000331134.10:c.96G>C ENSP00000331487.5:p.Lys32Asn
ENST00000374747.9:c.96G>C ENSP00000363879.5:p.Lys32Asn
ENST00000570300.1:n.117G>C
ENST00000574897.5:c.96G>C ENSP00000461543.1:p.Lys32Asn
ENST00000625705.1:c.93G>C ENSP00000486640.1:p.Lys31Asn
NM_017921.3:c.96G>C NP_060391.2:p.Lys32Asn
XM_011524979.1:c.96G>C XP_011523281.1:p.Lys32Asn
XM_011524980.1:c.96G>C XP_011523282.1:p.Lys32Asn
XM_011524981.1:c.96G>C XP_011523283.1:p.Lys32Asn
XM_011524982.1:c.96G>C XP_011523284.1:p.Lys32Asn
XR_934501.1:n.314G>C
XR_934502.1:n.314G>C
XM_011524982.2:c.96G>C XP_011523284.1:p.Lys32Asn
XR_001752557.1:n.314G>C
NM_017921.4:c.96G>C MANE Select NP_060391.2:p.Lys32Asn
NM_001369698.1:c.96G>C NP_001356627.1:p.Lys32Asn