Human (GRCh38.p14)
Description

DNA primase subunit 1 [Source:HGNC Symbol;Acc:HGNC:9369]

Location
About this transcript

This transcript has 13 exons, is annotated with 38 domains and features, is associated with 8821 variant alleles and maps to 388 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000338193.11PRIM1-2011423420aaENSP00000350491.5
 
Protein coding
CCDS44926P49642 NM_000946.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000672280.1PRIM1-2091875459aaENSP00000500157.1
 
Protein coding
A0A5F9ZHB6 -GENCODE basic
ENST00000706567.1PRIM1-2111684425aaENSP00000516452.1
 
Protein coding
--GENCODE basic
ENST00000550770.1PRIM1-2061008327aaENSP00000450185.1
 
Protein coding
F8VNY2 -TSL:5CDS 3' incomplete
ENST00000549549.1PRIM1-204456152aaENSP00000449806.1
 
Protein coding
H0YIP2 -TSL:3CDS 5' and 3' incomplete
ENST00000706566.1PRIM1-2101726420aaENSP00000516451.1
 
Nonsense mediated decay
CCDS44926---
ENST00000552590.6PRIM1-2081459185aaENSP00000448178.1
 
Nonsense mediated decay
F8VSB2 -TSL:5
ENST00000552408.1PRIM1-207566No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000546761.5PRIM1-202381No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000550224.5PRIM1-2051206No protein-
 
Retained intron
--TSL:5
ENST00000548173.5PRIM1-203590No protein-
 
Retained intron
--TSL:4
Statistics

Exons: 13, Coding exons: 13, Transcript length: 1,423 bps, Translation length: 420 residues

MANE

This MANE Select transcript contains ENSP00000350491 and matches to NM_000946.3 and NP_000937.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: P49642

CCDS

This transcript is a member of the Human CCDS set: CCDS44926

Transcript Support Level (TSL)

TSL:1

Version

ENST00000338193.11

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.