Linked Data
dbSNP Id:
rs1454370666
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149981717_149981721del , CM000667.2:g.149981717_149981721del | GRCh38 |
| NC_000005.9:g.149361280_149361284del , CM000667.1:g.149361280_149361284del | GRCh37 |
| NC_000005.8:g.149341473_149341477del | NCBI36 |
| NG_007147.2:g.22835_22839del , LRG_684:g.22835_22839del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000286298.5:c.2124_2128del MANE Select | ENSP00000286298.4:p.Phe709Ter | |
| ENST00000286298.4:c.2124_2128del | ENSP00000286298.4:p.Phe709Ter | |
| ENST00000503336.1:c.372+3366_372+3370del | ENSP00000426053.1:n.372+3366_372+3370del | |
| NM_000112.3:c.2124_2128del , LRG_684t1:c.2124_2128del | NP_000103.2:p.Phe709Ter | |
| XM_017009191.2:c.2124_2128del | XP_016864680.1:p.Phe709Ter | |
| NM_000112.4:c.2124_2128del MANE Select | NP_000103.2:p.Phe709Ter |