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Human (GRCh38.p14)
Description

fem-1 homolog B [Source:HGNC Symbol;Acc:HGNC:3649]

Location
About this transcript

This transcript has 2 exons, is annotated with 58 domains and features, is associated with 7542 variant alleles and maps to 436 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000306917.5FEM1B-2017177627aaENSP00000307298.4
 
Protein coding
CCDS10228Q9UK73 NM_015322.5MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000566008.1FEM1B-202878269aaENSP00000456968.1
 
Protein coding
H3BT12 -TSL:2CDS 5' incomplete
ENST00000570067.1FEM1B-2045794aaENSP00000457002.1
 
Protein coding
--TSL:4CDS 3' incomplete
ENST00000566739.1FEM1B-20357480aaENSP00000457342.1
 
Protein coding
H3BTV3 -TSL:4CDS 3' incomplete
Statistics

Exons: 2, Coding exons: 2, Transcript length: 7,177 bps, Translation length: 627 residues

MANE

This MANE Select transcript contains ENSP00000307298 and matches to NM_015322.5 and NP_056137.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9UK73

CCDS

This transcript is a member of the Human CCDS set: CCDS10228

Transcript Support Level (TSL)

TSL:1

Version

ENST00000306917.5

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.