solute carrier family 5 member 7 [Source:HGNC Symbol;Acc:HGNC:14025]
CHT, CHT1, HCHT
Chromosome 2: 107,986,523-108,013,994 forward strand.
GRCh38:CM000664.2
This gene has 2 transcripts (splice variants), 286 orthologues, 11 paralogues and is associated with 5 phenotypes.
Transcript ID | Name | bp | Protein | Translation ID | Biotype | CCDS | UniProt Match | RefSeq Match | Flags |
---|---|---|---|---|---|---|---|---|---|
ENST00000264047.3 | SLC5A7-201 | 5167 | 580aa | ENSP00000264047.2 | Protein coding | CCDS2074 | Q9GZV3 | NM_021815.5 | MANE Select, Ensembl Canonical, GENCODE basic, APPRIS P1, TSL:1, |
ENST00000409059.5 | SLC5A7-202 | 2032 | 580aa | ENSP00000387346.1 | Protein coding | CCDS2074 | Q9GZV3 | - | GENCODE basic, APPRIS P1, TSL:1, |