Canonical Allele Identifier: CA401463560

Gene: NPLOC4

Linked Data

• MyVariant Identifiers: chr17:g.79596813G>T (hg19) ; chr17:g.81629787G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000705719.1:c.163C>A	ENSP00000516165.1:p.Pro55Thr
ENST00000331134.11:c.34C>A MANE Select	ENSP00000331487.5:p.Pro12Thr
ENST00000331134.10:c.34C>A	ENSP00000331487.5:p.Pro12Thr
ENST00000374747.9:c.34C>A	ENSP00000363879.5:p.Pro12Thr
ENST00000570300.1:n.55C>A
ENST00000574897.5:c.34C>A	ENSP00000461543.1:p.Pro12Thr
ENST00000625705.1:c.31C>A	ENSP00000486640.1:p.Pro11Thr
NM_017921.3:c.34C>A	NP_060391.2:p.Pro12Thr
XM_011524979.1:c.34C>A	XP_011523281.1:p.Pro12Thr
XM_011524980.1:c.34C>A	XP_011523282.1:p.Pro12Thr
XM_011524981.1:c.34C>A	XP_011523283.1:p.Pro12Thr
XM_011524982.1:c.34C>A	XP_011523284.1:p.Pro12Thr
XR_934501.1:n.252C>A
XR_934502.1:n.252C>A
XM_011524982.2:c.34C>A	XP_011523284.1:p.Pro12Thr
XR_001752557.1:n.252C>A
NM_017921.4:c.34C>A MANE Select	NP_060391.2:p.Pro12Thr
NM_001369698.1:c.34C>A	NP_001356627.1:p.Pro12Thr