Canonical Allele Identifier: CA401463392

Gene: NPLOC4

Linked Data

• MyVariant Identifiers: chr17:g.79596761A>C (hg19) ; chr17:g.81629735A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81629735A>C , CM000679.2:g.81629735A>C	GRCh38
NC_000017.10:g.79596761A>C , CM000679.1:g.79596761A>C	GRCh37
NC_000017.9:g.77207166A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000705719.1:c.215T>G	ENSP00000516165.1:p.Phe72Cys
ENST00000331134.11:c.86T>G MANE Select	ENSP00000331487.5:p.Phe29Cys
ENST00000331134.10:c.86T>G	ENSP00000331487.5:p.Phe29Cys
ENST00000374747.9:c.86T>G	ENSP00000363879.5:p.Phe29Cys
ENST00000570300.1:n.107T>G
ENST00000574897.5:c.86T>G	ENSP00000461543.1:p.Phe29Cys
ENST00000625705.1:c.83T>G	ENSP00000486640.1:p.Phe28Cys
NM_017921.3:c.86T>G	NP_060391.2:p.Phe29Cys
XM_011524979.1:c.86T>G	XP_011523281.1:p.Phe29Cys
XM_011524980.1:c.86T>G	XP_011523282.1:p.Phe29Cys
XM_011524981.1:c.86T>G	XP_011523283.1:p.Phe29Cys
XM_011524982.1:c.86T>G	XP_011523284.1:p.Phe29Cys
XR_934501.1:n.304T>G
XR_934502.1:n.304T>G
XM_011524982.2:c.86T>G	XP_011523284.1:p.Phe29Cys
XR_001752557.1:n.304T>G
NM_017921.4:c.86T>G MANE Select	NP_060391.2:p.Phe29Cys
NM_001369698.1:c.86T>G	NP_001356627.1:p.Phe29Cys