Linked Data
dbSNP Id:
rs1755020856
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149977911_149977912insTA , CM000667.2:g.149977911_149977912insTA | GRCh38 |
| NC_000005.9:g.149357474_149357475insTA , CM000667.1:g.149357474_149357475insTA | GRCh37 |
| NC_000005.8:g.149337667_149337668insTA | NCBI36 |
| NG_007147.2:g.19029_19030insTA , LRG_684:g.19029_19030insTA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000690410.1:n.491_492insTA | ||
| ENST00000286298.5:c.259_260insTA MANE Select | ENSP00000286298.4:p.Asn87IlefsTer3 | |
| ENST00000286298.4:c.259_260insTA | ENSP00000286298.4:p.Asn87IlefsTer3 | |
| NM_000112.3:c.259_260insTA , LRG_684t1:c.259_260insTA | NP_000103.2:p.Asn87IlefsTer3 | |
| XM_017009191.2:c.259_260insTA | XP_016864680.1:p.Asn87IlefsTer3 | |
| NM_000112.4:c.259_260insTA MANE Select | NP_000103.2:p.Asn87IlefsTer3 |