Human (GRCh38.p14)
Description

myelin regulatory factor like [Source:HGNC Symbol;Acc:HGNC:26316]

Gene Synonyms

BCM1377, C12ORF15, C12ORF28, FLJ25056

Location
About this transcript

This transcript has 25 exons, is annotated with 18 domains and features, is associated with 57515 variant alleles and maps to 681 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000552032.7MYRFL-2053590910aaENSP00000448753.2
 
Protein coding
CCDS76577Q96LU7 NM_182530.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P2TSL:5
ENST00000547771.6MYRFL-2033465898aaENSP00000449598.2
 
Protein coding
F8VVR8 -GENCODE basicAPPRIS ALT2TSL:5
ENST00000548892.5MYRFL-2041319375aaENSP00000447167.1
 
Protein coding
H0YHI9 -TSL:2CDS 5' incomplete
ENST00000535034.5MYRFL-202881250aaENSP00000440626.1
 
Protein coding
F5GYH9 -GENCODE basicTSL:1
ENST00000299350.5MYRFL-201820250aaENSP00000299350.5
 
Protein coding
A0A075B6E6 -GENCODE basicTSL:5
Statistics

Exons: 25, Coding exons: 25, Transcript length: 3,590 bps, Translation length: 910 residues

MANE

This MANE Select transcript contains ENSP00000448753 and matches to NM_182530.3 and NP_872336.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q96LU7

CCDS

This transcript is a member of the Human CCDS set: CCDS76577

Transcript Support Level (TSL)

TSL:5

Version

ENST00000552032.7

Type

Protein coding

Annotation Method

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

Annotation Attributes

not organism-supported [Definitions]

GENCODE basic gene

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