Canonical Allele Identifier: CA502298209
Gene: NPLOC4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.79596814G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81629788G>T , CM000679.2:g.81629788G>T GRCh38
NC_000017.10:g.79596814G>T , CM000679.1:g.79596814G>T GRCh37
NC_000017.9:g.77207219G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000705719.1:c.162C>A ENSP00000516165.1:p.Ser54=
ENST00000331134.11:c.33C>A MANE Select ENSP00000331487.5:p.Ser11=
ENST00000331134.10:c.33C>A ENSP00000331487.5:p.Ser11=
ENST00000374747.9:c.33C>A ENSP00000363879.5:p.Ser11=
ENST00000570300.1:n.54C>A
ENST00000574897.5:c.33C>A ENSP00000461543.1:p.Ser11=
ENST00000625705.1:c.30C>A ENSP00000486640.1:p.Ser10=
NM_017921.3:c.33C>A NP_060391.2:p.Ser11=
XM_011524979.1:c.33C>A XP_011523281.1:p.Ser11=
XM_011524980.1:c.33C>A XP_011523282.1:p.Ser11=
XM_011524981.1:c.33C>A XP_011523283.1:p.Ser11=
XM_011524982.1:c.33C>A XP_011523284.1:p.Ser11=
XR_934501.1:n.251C>A
XR_934502.1:n.251C>A
XM_011524982.2:c.33C>A XP_011523284.1:p.Ser11=
XR_001752557.1:n.251C>A
NM_017921.4:c.33C>A MANE Select NP_060391.2:p.Ser11=
NM_001369698.1:c.33C>A NP_001356627.1:p.Ser11=