Canonical Allele Identifier: CA2278608418

Gene: NPLOC4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81629787G= , CM000679.2:g.81629787G=	GRCh38
NC_000017.10:g.79596813G= , CM000679.1:g.79596813G=	GRCh37
NC_000017.9:g.77207218G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000705719.1:c.163C=	ENSP00000516165.1:p.Pro55=
ENST00000331134.11:c.34C= MANE Select	ENSP00000331487.5:p.Pro12=
ENST00000331134.10:c.34C=	ENSP00000331487.5:p.Pro12=
ENST00000374747.9:c.34C=	ENSP00000363879.5:p.Pro12=
ENST00000570300.1:n.55C=
ENST00000574897.5:c.34C=	ENSP00000461543.1:p.Pro12=
ENST00000625705.1:c.31C=	ENSP00000486640.1:p.Pro11=
NM_017921.3:c.34C=	NP_060391.2:p.Pro12=
XM_011524979.1:c.34C=	XP_011523281.1:p.Pro12=
XM_011524980.1:c.34C=	XP_011523282.1:p.Pro12=
XM_011524981.1:c.34C=	XP_011523283.1:p.Pro12=
XM_011524982.1:c.34C=	XP_011523284.1:p.Pro12=
XR_934501.1:n.252C=
XR_934502.1:n.252C=
XM_011524982.2:c.34C=	XP_011523284.1:p.Pro12=
XR_001752557.1:n.252C=
NM_017921.4:c.34C= MANE Select	NP_060391.2:p.Pro12=
NM_001369698.1:c.34C=	NP_001356627.1:p.Pro12=