Canonical Allele Identifier: CA502298174

Gene: NPLOC4

Linked Data

• gnomAD v4: 17-81629743-T-C
• MyVariant Identifiers: chr17:g.79596769T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81629743T>C , CM000679.2:g.81629743T>C	GRCh38
NC_000017.10:g.79596769T>C , CM000679.1:g.79596769T>C	GRCh37
NC_000017.9:g.77207174T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000705719.1:c.207A>G	ENSP00000516165.1:p.Ala69=
ENST00000331134.11:c.78A>G MANE Select	ENSP00000331487.5:p.Ala26=
ENST00000331134.10:c.78A>G	ENSP00000331487.5:p.Ala26=
ENST00000374747.9:c.78A>G	ENSP00000363879.5:p.Ala26=
ENST00000570300.1:n.99A>G
ENST00000574897.5:c.78A>G	ENSP00000461543.1:p.Ala26=
ENST00000625705.1:c.75A>G	ENSP00000486640.1:p.Ala25=
NM_017921.3:c.78A>G	NP_060391.2:p.Ala26=
XM_011524979.1:c.78A>G	XP_011523281.1:p.Ala26=
XM_011524980.1:c.78A>G	XP_011523282.1:p.Ala26=
XM_011524981.1:c.78A>G	XP_011523283.1:p.Ala26=
XM_011524982.1:c.78A>G	XP_011523284.1:p.Ala26=
XR_934501.1:n.296A>G
XR_934502.1:n.296A>G
XM_011524982.2:c.78A>G	XP_011523284.1:p.Ala26=
XR_001752557.1:n.296A>G
NM_017921.4:c.78A>G MANE Select	NP_060391.2:p.Ala26=
NM_001369698.1:c.78A>G	NP_001356627.1:p.Ala26=