Human (GRCh38.p14)
Description

coiled-coil domain containing 197 [Source:HGNC Symbol;Acc:HGNC:19860]

Gene Synonyms

C14ORF48, LINC00521

Location
About this transcript

This transcript has 7 exons, is annotated with 5 domains and features, is associated with 5229 variant alleles and maps to 337 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000636493.2CCDC197-2051274272aaENSP00000490086.1
 
Protein coding
CCDS86426A0A1B0GUF5 NM_001351596.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P2TSL:5
ENST00000640978.1CCDC197-2061429222aaENSP00000491594.1
 
Protein coding
CCDS91922A0A1W2PPK9 -GENCODE basicAPPRIS ALT2TSL:5
ENST00000444118.5CCDC197-202193790aaENSP00000489802.1
 
Nonsense mediated decay
A0A1B0GTQ9 -TSL:1
ENST00000359253.2CCDC197-2011275143aaENSP00000490490.1
 
Nonsense mediated decay
Q8NCU1-1 -TSL:1
ENST00000449472.1CCDC197-203477No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000455802.5CCDC197-204427No protein-
 
Protein coding CDS not defined
--TSL:5
Statistics

Exons: 7, Coding exons: 6, Transcript length: 1,274 bps, Translation length: 272 residues

MANE

This MANE Select transcript contains ENSP00000490086 and matches to NM_001351596.2 and NP_001338525.1

CCDS

This transcript is a member of the Human CCDS set: CCDS86426

Transcript Support Level (TSL)

TSL:5

Version

ENST00000636493.2

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

Annotation Attributes

inferred exon combination [Definitions]

RNA-Seq supported only

GENCODE basic gene

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