Human (GRCh38.p14)
Description

death domain containing 1 [Source:HGNC Symbol;Acc:HGNC:37261]

Gene Synonyms

FLJ16686

Location
About this transcript

This transcript has 10 exons, is annotated with 13 domains and features, is associated with 27226 variant alleles and maps to 440 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000639862.2DTHD1-2066551906aaENSP00000492542.1
 
Protein coding
CCDS54754A0A1W2PR94 NM_001170700.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P2TSL:5
ENST00000456874.3DTHD1-2023365781aaENSP00000401597.2
 
Protein coding
Q6ZMT9-1 -GENCODE basicAPPRIS ALT2TSL:1
ENST00000357504.7DTHD1-2013203616aaENSP00000350103.3
 
Protein coding
Q6ZMT9-2 -GENCODE basicAPPRIS ALT2TSL:2
ENST00000507598.5DTHD1-2052606821aaENSP00000424426.1
 
Protein coding
D6RB49 -GENCODE basicAPPRIS ALT2TSL:1
ENST00000503528.1DTHD1-2032761No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000506008.1DTHD1-204453No protein-
 
Protein coding CDS not defined
--TSL:3
Statistics

Exons: 10, Coding exons: 10, Transcript length: 6,551 bps, Translation length: 906 residues

MANE

This MANE Select transcript contains ENSP00000492542 and matches to NM_001170700.3 and NP_001164171.2

CCDS

This transcript is a member of the Human CCDS set: CCDS54754

Transcript Support Level (TSL)

TSL:5

Version

ENST00000639862.2

Type

Protein coding

Annotation Method

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

Annotation Attributes

inferred transcript model [Definitions]

RNA-Seq supported partial

GENCODE basic gene

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