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Human (GRCh38.p14)
Description

serum amyloid A2 [Source:HGNC Symbol;Acc:HGNC:10514]

Location

Chromosome 11: 18,239,223-18,248,668 reverse strand.

GRCh38:CM000673.2

About this gene

This gene has 6 transcripts (splice variants), 147 orthologues and 3 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000256733.9SAA2-201576122aaENSP00000256733.5
 
Protein coding
CCDS7833P0DJI9-1 NM_030754.5MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000414546.6SAA2-202102283aaENSP00000416716.2
 
Protein coding
CCDS44548P0DJI9-2 -GENCODE BasicTSL:1
ENST00000528349.5SAA2-204948113aaENSP00000435659.1
 
Protein coding
G3V1D9 -GENCODE BasicTSL:2
ENST00000526900.1SAA2-203687122aaENSP00000436126.1
 
Protein coding
CCDS7833P0DJI9-1 -GENCODE BasicAPPRIS P1TSL:2
ENST00000529528.5SAA2-205610122aaENSP00000437162.1
 
Protein coding
CCDS7833P0DJI9-1 -GENCODE PrimaryGENCODE BasicAPPRIS P1TSL:2
ENST00000530400.5SAA2-20632380aaENSP00000432370.1
 
Protein coding
E9PR14 -GENCODE BasicTSL:3