Canonical Allele Identifier: CA2278608398

Gene: NPLOC4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81629725_81629726delinsCT , CM000679.2:g.81629725_81629726delinsCT	GRCh38
NC_000017.10:g.79596751_79596752delinsCT , CM000679.1:g.79596751_79596752delinsCT	GRCh37
NC_000017.9:g.77207156_77207157delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000705719.1:c.224_225delinsAG	ENSP00000516165.1:p.Lys75=
ENST00000331134.11:c.95_96delinsAG MANE Select	ENSP00000331487.5:p.Lys32=
ENST00000331134.10:c.95_96delinsAG	ENSP00000331487.5:p.Lys32=
ENST00000374747.9:c.95_96delinsAG	ENSP00000363879.5:p.Lys32=
ENST00000570300.1:n.116_117delinsAG
ENST00000574897.5:c.95_96delinsAG	ENSP00000461543.1:p.Lys32=
ENST00000625705.1:c.92_93delinsAG	ENSP00000486640.1:p.Lys31=
NM_017921.3:c.95_96delinsAG	NP_060391.2:p.Lys32=
XM_011524979.1:c.95_96delinsAG	XP_011523281.1:p.Lys32=
XM_011524980.1:c.95_96delinsAG	XP_011523282.1:p.Lys32=
XM_011524981.1:c.95_96delinsAG	XP_011523283.1:p.Lys32=
XM_011524982.1:c.95_96delinsAG	XP_011523284.1:p.Lys32=
XR_934501.1:n.313_314delinsAG
XR_934502.1:n.313_314delinsAG
XM_011524982.2:c.95_96delinsAG	XP_011523284.1:p.Lys32=
XR_001752557.1:n.313_314delinsAG
NM_017921.4:c.95_96delinsAG MANE Select	NP_060391.2:p.Lys32=
NM_001369698.1:c.95_96delinsAG	NP_001356627.1:p.Lys32=