Linked Data
dbSNP Id:
rs2125314772
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.38071095del , CM000664.2:g.38071095del | GRCh38 |
| NC_000002.11:g.38298238del , CM000664.1:g.38298238del | GRCh37 |
| NC_000002.10:g.38151742del | NCBI36 |
| NG_008386.2:g.10011del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000490576.2:c.1263del | ENSP00000478839.2:p.Phe421LeufsTer7 | |
| ENST00000610745.5:c.1263del MANE Select | ENSP00000478561.1:p.Phe421LeufsTer7 | |
| ENST00000492443.1:n.641del | ||
| ENST00000494864.1:c.150del | ENSP00000479876.1:p.Phe50LeufsTer7 | |
| ENST00000610745.4:c.1263del | ENSP00000478561.1:p.Phe421LeufsTer7 | |
| ENST00000614273.1:c.1263del | ENSP00000483678.1:p.Phe421LeufsTer7 | |
| NM_000104.3:c.1263del | NP_000095.2:p.Phe421LeufsTer7 | |
| NM_000104.4:c.1263del MANE Select | NP_000095.2:p.Phe421LeufsTer7 |