Canonical Allele Identifier: CA401463370
Gene: NPLOC4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.79596752T>G (hg19) chr17:g.81629726T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81629726T>G , CM000679.2:g.81629726T>G GRCh38
NC_000017.10:g.79596752T>G , CM000679.1:g.79596752T>G GRCh37
NC_000017.9:g.77207157T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000705719.1:c.224A>C ENSP00000516165.1:p.Lys75Thr
ENST00000331134.11:c.95A>C MANE Select ENSP00000331487.5:p.Lys32Thr
ENST00000331134.10:c.95A>C ENSP00000331487.5:p.Lys32Thr
ENST00000374747.9:c.95A>C ENSP00000363879.5:p.Lys32Thr
ENST00000570300.1:n.116A>C
ENST00000574897.5:c.95A>C ENSP00000461543.1:p.Lys32Thr
ENST00000625705.1:c.92A>C ENSP00000486640.1:p.Lys31Thr
NM_017921.3:c.95A>C NP_060391.2:p.Lys32Thr
XM_011524979.1:c.95A>C XP_011523281.1:p.Lys32Thr
XM_011524980.1:c.95A>C XP_011523282.1:p.Lys32Thr
XM_011524981.1:c.95A>C XP_011523283.1:p.Lys32Thr
XM_011524982.1:c.95A>C XP_011523284.1:p.Lys32Thr
XR_934501.1:n.313A>C
XR_934502.1:n.313A>C
XM_011524982.2:c.95A>C XP_011523284.1:p.Lys32Thr
XR_001752557.1:n.313A>C
NM_017921.4:c.95A>C MANE Select NP_060391.2:p.Lys32Thr
NM_001369698.1:c.95A>C NP_001356627.1:p.Lys32Thr
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