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Human (GRCh38.p14)
Description

Rh family C glycoprotein [Source:HGNC Symbol;Acc:HGNC:18140]

Gene Synonyms

C15ORF6, PDRC2, RHGK, SLC42A3

Location
About this transcript

This transcript has 11 exons, is annotated with 54 domains and features, is associated with 12326 variant alleles and maps to 384 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000268122.9RHCG-2011952479aaENSP00000268122.4
 
Protein coding
CCDS10351Q9UBD6 NM_016321.3MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000558360.1RHCG-2041014237aaENSP00000453496.1
 
Protein coding
H0YM79 -TSL:2CDS 5' incomplete
ENST00000649642.1RHCG-2071909417aaENSP00000497611.1
 
Nonsense mediated decay
A0A3B3IT41 --
ENST00000560081.5RHCG-2061862331aaENSP00000453588.1
 
Nonsense mediated decay
H0YMF8 -TSL:1
ENST00000558030.5RHCG-2021405233aaENSP00000452899.1
 
Nonsense mediated decay
H0YKQ3 -TSL:5
ENST00000558184.1RHCG-2031388136aaENSP00000453716.1
 
Nonsense mediated decay
H0YMS1 -TSL:1
ENST00000559638.1RHCG-205591No protein-
 
Retained intron
--TSL:3
Statistics

Exons: 11, Coding exons: 10, Transcript length: 1,952 bps, Translation length: 479 residues

MANE

This MANE Select transcript contains ENSP00000268122 and matches to NM_016321.3 and NP_057405.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9UBD6

CCDS

This transcript is a member of the Human CCDS set: CCDS10351

Transcript Support Level (TSL)

TSL:1

Version

ENST00000268122.9

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.

GENCODE primary gene

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