Canonical Allele Identifier: CA986866570

Gene: NPLOC4

Linked Data

• dbSNP Id: rs2035887090
• gnomAD v3: 17-81629909-TA-T
• gnomAD v4: 17-81629909-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81629912del , CM000679.2:g.81629912del	GRCh38
NC_000017.10:g.79596938del , CM000679.1:g.79596938del	GRCh37
NC_000017.9:g.77207343del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000705719.1:c.145-105del	ENSP00000516165.1:n.145-105del
ENST00000331134.11:c.16-105del MANE Select	ENSP00000331487.5:n.16-105del
ENST00000331134.10:c.16-105del	ENSP00000331487.5:n.16-105del
ENST00000374747.9:c.16-105del	ENSP00000363879.5:n.16-105del
ENST00000570300.1:n.37-105del
ENST00000574897.5:c.16-105del	ENSP00000461543.1:n.16-105del
NM_017921.3:c.16-105del	NP_060391.2:n.16-105del
XM_011524979.1:c.16-105del	XP_011523281.1:n.16-105del
XM_011524980.1:c.16-105del	XP_011523282.1:n.16-105del
XM_011524981.1:c.16-105del	XP_011523283.1:n.16-105del
XM_011524982.1:c.16-105del	XP_011523284.1:n.16-105del
XR_934501.1:n.234-105del
XR_934502.1:n.234-105del
XM_011524982.2:c.16-105del	XP_011523284.1:n.16-105del
XR_001752557.1:n.234-105del
NM_017921.4:c.16-105del MANE Select	NP_060391.2:n.16-105del
NM_001369698.1:c.16-105del	NP_001356627.1:n.16-105del