Linked Data
dbSNP Id:
rs1161610169
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.47286311_47286314del , CM000679.2:g.47286311_47286314del | GRCh38 |
| NC_000017.10:g.45363677_45363680del , CM000679.1:g.45363677_45363680del | GRCh37 |
| NC_000017.9:g.42718676_42718679del | NCBI36 |
| NG_008332.2:g.37470_37473del , LRG_481:g.37470_37473del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696963.1:c.666_669del | ENSP00000513002.1:p.Asp224ArgfsTer2 | |
| ENST00000559488.7:c.666_669del MANE Select | ENSP00000452786.2:p.Asp224ArgfsTer2 | |
| ENST00000559488.5:c.666_669del | ENSP00000452786.1:p.Asp224ArgfsTer2 | |
| ENST00000560629.1:c.631_634del | ||
| ENST00000571680.1:c.666_669del | ENSP00000461626.1:p.Asp224ArgfsTer2 | |
| NM_000212.2:c.666_669del , LRG_481t1:c.666_669del | NP_000203.2:p.Asp224ArgfsTer2 | |
| NM_000212.3:c.666_669del MANE Select | NP_000203.2:p.Asp224ArgfsTer2 |